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- NCIT_C101145 IAO_0000115 "Human SYP wild-type allele is located within Xp11.23-p11.22 and is approximately 12 kb in length. This allele, which encodes synaptophysin protein, plays a role in synaptic functions. Mutation of the gene is associated with SYP-related mental retardation X-linked." @default.
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- NCIT_C101145 NCIT_P100 "313475" @default.
- NCIT_C101145 NCIT_P102 "X06389" @default.
- NCIT_C101145 NCIT_P106 "Gene or Genome" @default.
- NCIT_C101145 NCIT_P107 "SYP wt Allele" @default.
- NCIT_C101145 NCIT_P108 "SYP wt Allele" @default.
- NCIT_C101145 NCIT_P207 "C3539703" @default.
- NCIT_C101145 NCIT_P321 "6855" @default.
- NCIT_C101145 NCIT_P322 "CTRP" @default.
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- NCIT_C101145 hasExactSynonym "MRX96" @default.
- NCIT_C101145 hasExactSynonym "MRXSYP" @default.
- NCIT_C101145 hasExactSynonym "SYP wt Allele" @default.
- NCIT_C101145 hasExactSynonym "Synaptophysin wt Allele" @default.
- NCIT_C101145 inSubset NCIT_C116977 @default.
- NCIT_C101145 inSubset NCIT_C142799 @default.
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- NCIT_C101145 type Class @default.
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- NCIT_C101145 label "SYP wt Allele" @default.
- NCIT_C101145 subClassOf NCIT_C101144 @default.
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