Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_assertion> ?p ?o ?g. }
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- NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_assertion type Assertion NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_head.
- 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.