Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance.
- NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_assertion description "[Although mutations in MYH14 have been shown to cause nonsyndromic autosomal dominant hearing loss (DFNA4), the peripheral neuropathy, myopathy, and hoarseness have not been associated with MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance.
- NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_assertion evidence source_evidence_literature NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance.
- NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_assertion SIO_000772 21480433 NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance.
- NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_assertion wasDerivedFrom befree-20150227 NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance.
- NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_assertion wasGeneratedBy ECO_0000203 NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP945560.RAVOSuMhtnMOTJpC4SOLijL5c1_l16-yInBS9cdz58hw4130_provenance.