Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_assertion> ?p ?o ?g. }
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- NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_assertion type Assertion NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_head.
- NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_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." NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance.
- NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_assertion evidence source_evidence_literature NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance.
- NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_assertion SIO_000772 15889046 NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance.
- NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_assertion wasDerivedFrom befree-20140225 NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance.
- NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_assertion wasGeneratedBy ECO_0000203 NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance.