Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion wasGeneratedBy ECO_0000203 NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion wasDerivedFrom befree-2016 NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion SIO_000772 23434763 NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion evidence source_evidence_literature NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion description "[Recessive inactivating mutations in WNT1 are a new cause of OI type IV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.