Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP189977.RAEBQrwfXDnZbpejUXxsvRrvizHldlEsbqlxbXZmhcXys130_provenance.