Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance.
- NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_assertion description "[Five non-syndromic deaf individuals were identified with normal retinal and vestibular phenotypes that segregate compound heterozygous mutations of CDH23, where one mutation is a known or predicted USH1 allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance.
- NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_assertion evidence source_evidence_literature NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance.
- NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_assertion SIO_000772 21940737 NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance.
- NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_assertion wasDerivedFrom befree-20150227 NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance.
- NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_assertion wasGeneratedBy ECO_0000203 NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936931.RAmvAqdbUlxHa4TQSUV8gY3m1wT3-CMywg2k3HsBDIrjE130_provenance.