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- NCIT_C114411 IAO_0000115 "Human PLXND1 wild-type allele is located in the vicinity of 3q22.1 and is approximately 52 kb in length. This allele, which encodes plexin-D1 protein, plays a role in semaphorin-mediated signaling." @default.
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- NCIT_C114411 NCIT_P100 "604282" @default.
- NCIT_C114411 NCIT_P102 "AY116661" @default.
- NCIT_C114411 NCIT_P106 "Gene or Genome" @default.
- NCIT_C114411 NCIT_P107 "PLXND1 wt Allele" @default.
- NCIT_C114411 NCIT_P108 "PLXND1 wt Allele" @default.
- NCIT_C114411 NCIT_P207 "C3815264" @default.
- NCIT_C114411 NCIT_P321 "23129" @default.
- NCIT_C114411 NCIT_P322 "CTRP" @default.
- NCIT_C114411 NCIT_P98 "There is a report of a chromosomal aberration involving the PLXND1 gene and the TMCC1 gene, which is associated with breast cancer. (COSMIC)" @default.
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- NCIT_C114411 normalizedInformationContent "100" @default.
- NCIT_C114411 referenceCount "1" @default.
- NCIT_C114411 hasExactSynonym "KIAA0620" @default.
- NCIT_C114411 hasExactSynonym "PLEXD1" @default.
- NCIT_C114411 hasExactSynonym "PLXND1 wt Allele" @default.
- NCIT_C114411 hasExactSynonym "Plexin D1 wt Allele" @default.
- NCIT_C114411 inSubset NCIT_C116977 @default.
- NCIT_C114411 inSubset NCIT_C142799 @default.
- NCIT_C114411 inSubset NCIT_C142800 @default.
- NCIT_C114411 type Class @default.
- NCIT_C114411 isDefinedBy ncit.owl @default.
- NCIT_C114411 label "PLXND1 wt Allele" @default.
- NCIT_C114411 subClassOf Bb766b76167cf1f8aa16ffecf26cd520f @default.
- NCIT_C114411 subClassOf Be913af5fa4db8500a567d9d03638338d @default.
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- NCIT_C114411 subClassOf NCIT_C114411 @default.
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- NCIT_C114411 subClassOf NCIT_C20103 @default.
- NCIT_C114411 subClassOf NCIT_C21295 @default.