Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_assertion> ?p ?o ?g. }
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- NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_assertion type Assertion NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_head.
- NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_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." NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_provenance.
- NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_assertion evidence source_evidence_literature NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_provenance.
- NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_assertion SIO_000772 15889046 NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_provenance.
- NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_assertion wasDerivedFrom befree-20150227 NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_provenance.
- NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_assertion wasGeneratedBy ECO_0000203 NP601445.RACqdleEQr9f8DDI0pBYUR-MSXRp2Lf13mthBNaWrNfNA130_provenance.