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- NCIT_C176522 IAO_0000115 "Human HNRNPH2 wild-type allele is located in the vicinity of Xq22.1 and is approximately 6 kb in length. This allele, which encodes heterogeneous nuclear ribonucleoprotein H2, plays a role in the maturation of messenger RNA. Mutation of the gene is associated with the Bain type of X-linked syndromic mental retardation and may be associated with Fabray disease and X-linked agammaglobulinemia." @default.
- NCIT_C176522 NCIT_NHC0 "C176522" @default.
- NCIT_C176522 NCIT_P100 "300610" @default.
- NCIT_C176522 NCIT_P102 "U01923" @default.
- NCIT_C176522 NCIT_P106 "Gene or Genome" @default.
- NCIT_C176522 NCIT_P108 "HNRNPH2 wt Allele" @default.
- NCIT_C176522 NCIT_P208 "CL1642369" @default.
- NCIT_C176522 NCIT_P321 "3188" @default.
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- NCIT_C176522 NCIT_R37 NCIT_C19986 @default.
- NCIT_C176522 NCIT_R37 NCIT_C20139 @default.
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- NCIT_C176522 NCIT_R37 NCIT_C28498 @default.
- NCIT_C176522 NCIT_R37 NCIT_C40523 @default.
- NCIT_C176522 NCIT_R40 NCIT_C12219 @default.
- NCIT_C176522 NCIT_R40 NCIT_C13282 @default.
- NCIT_C176522 NCIT_R40 NCIT_C13377 @default.
- NCIT_C176522 NCIT_R40 NCIT_C13432 @default.
- NCIT_C176522 NCIT_R40 NCIT_C13446 @default.
- NCIT_C176522 NCIT_R40 NCIT_C13792 @default.
- NCIT_C176522 NCIT_R40 NCIT_C14135 @default.
- NCIT_C176522 NCIT_R40 NCIT_C32221 @default.
- NCIT_C176522 NCIT_R40 NCIT_C34070 @default.
- NCIT_C176522 NCIT_R41 NCIT_C14182 @default.
- NCIT_C176522 NCIT_R41 NCIT_C14225 @default.
- NCIT_C176522 NCIT_R41 NCIT_C14234 @default.
- NCIT_C176522 NCIT_R41 NCIT_C14250 @default.
- NCIT_C176522 NCIT_R41 NCIT_C14262 @default.
- NCIT_C176522 NCIT_R41 NCIT_C14282 @default.
- NCIT_C176522 NCIT_R41 NCIT_C25796 @default.
- NCIT_C176522 NCIT_R41 NCIT_C79740 @default.
- NCIT_C176522 normalizedInformationContent "100" @default.
- NCIT_C176522 referenceCount "1" @default.
- NCIT_C176522 hasExactSynonym "FTP3" @default.
- NCIT_C176522 hasExactSynonym "HNRNPH2 wt Allele" @default.
- NCIT_C176522 hasExactSynonym "HNRPH'" @default.
- NCIT_C176522 hasExactSynonym "HNRPH2" @default.
- NCIT_C176522 hasExactSynonym "Heterogeneous Nuclear Ribonucleoprotein H' Gene" @default.
- NCIT_C176522 hasExactSynonym "Heterogeneous Nuclear Ribonucleoprotein H-Prime Gene" @default.
- NCIT_C176522 hasExactSynonym "Heterogeneous Nuclear Ribonucleoprotein H2 (H') Gene" @default.
- NCIT_C176522 hasExactSynonym "Heterogeneous Nuclear Ribonucleoprotein H2 wt Allele" @default.
- NCIT_C176522 hasExactSynonym "MRXSB" @default.
- NCIT_C176522 hasExactSynonym "NRPH2" @default.
- NCIT_C176522 hasExactSynonym "hnRNPH'" @default.
- NCIT_C176522 type Class @default.
- NCIT_C176522 isDefinedBy ncit.owl @default.
- NCIT_C176522 label "HNRNPH2 wt Allele" @default.
- NCIT_C176522 subClassOf Ba831b2359573ad870c7597c81baf75ca @default.
- NCIT_C176522 subClassOf Be92bd24449297e83f6b8bc6fe199f55f @default.
- NCIT_C176522 subClassOf NCIT_C16612 @default.
- NCIT_C176522 subClassOf NCIT_C176521 @default.
- NCIT_C176522 subClassOf NCIT_C176522 @default.
- NCIT_C176522 subClassOf NCIT_C21295 @default.