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- NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_assertion type Assertion NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_head.
- NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_assertion description "[The occuloalbinism 2 (OCA2) gene, localized at 15q11, encodes a melanosomal transmembrane protein that is involved in the most common form of human occulo-cutaneous albinism, a human genetic disorder characterized by fair pigmentation and susceptibility to skin cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_provenance.
- NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_assertion evidence source_evidence_literature NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_provenance.
- NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_assertion SIO_000772 15889046 NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_provenance.
- NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_assertion wasDerivedFrom befree-20140225 NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_provenance.
- NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_assertion wasGeneratedBy ECO_0000203 NP938500.RACwZp7SvM48Ad9kM_7Kf6vLvx_VL3bZgNfDN7yos4meU130_provenance.