Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance.
- NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_assertion description "[OCA3 was thought to be restricted to black populations, where it was clinically described as rufous or brown albinism, until the recent report of a homozygous TYRP1 mutation in Caucasian patients from a consanguineous Pakistani family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance.
- NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_assertion evidence source_evidence_literature NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance.
- NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_assertion SIO_000772 16704458 NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance.
- NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_assertion wasDerivedFrom befree-20140225 NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance.
- NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_assertion wasGeneratedBy ECO_0000203 NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP750251.RA_OK9Zh3ioc17q-CqKPS276UevQreFNbFYcksoxoh3nc130_provenance.