Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance.
- NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_assertion wasGeneratedBy ECO_0000203 NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance.
- NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_assertion wasDerivedFrom befree-20150227 NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance.
- NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_assertion SIO_000772 16550584 NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance.
- NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_assertion evidence source_evidence_literature NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance.
- NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_assertion description "[One of these genes, cadherin 23, produces a spectrum of phenotypic traits, including presbycusis, nonsyndromic prelingual hearing loss (DFNB12), and syndromic hearing loss as part of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936907.RACqrD0gUE0ji_x5O1Q0GPBFulSWoaj6Y-xntvTuIM-cM130_provenance.