Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.
- NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_assertion wasGeneratedBy ECO_0000203 NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.
- NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_assertion wasDerivedFrom befree-20140225 NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.
- NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_assertion SIO_000772 18429043 NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.
- NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_assertion evidence source_evidence_literature NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.
- NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.