Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance.
- NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_assertion description "[Together, these data suggest that SLC26A4, FOXI1 and KCNJ10 are not major determinants in unilateral deafness and enlarged vestibular aqueduct compared with their implication in Pendred syndrome and non-syndromic bilateral enlarged vestibular aqueduct.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance.
- NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_assertion evidence source_evidence_literature NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance.
- NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_assertion SIO_000772 20621367 NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance.
- NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_assertion wasDerivedFrom befree-20140225 NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance.
- NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_assertion wasGeneratedBy ECO_0000203 NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP612085.RAyYbg3H7e7OtPrCKsWzzp9Rt0CnfOD0DI8ZI5NzfWzfw130_provenance.