Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance.
- NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_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." NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance.
- NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_assertion evidence source_evidence_literature NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance.
- NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_assertion SIO_000772 16704458 NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance.
- NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_assertion wasDerivedFrom befree-20150227 NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance.
- NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_assertion wasGeneratedBy ECO_0000203 NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP764389.RATjX6my-TGJMfozY6i89Mw-MAQKNuByQs09FbDtUd7d4130_provenance.