Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance.
- NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_assertion description "[Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance.
- NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_assertion evidence source_evidence_literature NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance.
- NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_assertion SIO_000772 11574907 NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance.
- NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_assertion wasDerivedFrom befree-20140225 NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance.
- NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_assertion wasGeneratedBy ECO_0000203 NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP265494.RAemPFCH9keK3mO4jzqKApPYQIPtVCWNV7wt2_WkTnKMI130_provenance.