Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_assertion> ?p ?o ?g. }
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- NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_assertion type Assertion NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_head.
- NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_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." NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_provenance.
- NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_assertion evidence source_evidence_literature NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_provenance.
- NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_assertion SIO_000772 15889046 NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_provenance.
- NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_assertion wasDerivedFrom befree-2016 NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_provenance.
- NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_assertion wasGeneratedBy ECO_0000203 NP494438.RAtiRwc9j-5gkevoSxuoOAH4yNqmzFlTRyIq2K6nRNN6M130_provenance.