Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.
- NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.
- NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_assertion evidence source_evidence_literature NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.
- NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_assertion SIO_000772 21480433 NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.
- NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_assertion wasDerivedFrom befree-20140225 NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.
- NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_assertion wasGeneratedBy ECO_0000203 NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.