Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance.
- NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_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." NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance.
- NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_assertion evidence source_evidence_literature NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance.
- NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_assertion SIO_000772 21480433 NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance.
- NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_assertion wasDerivedFrom befree-20140225 NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance.
- NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_assertion wasGeneratedBy ECO_0000203 NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP608342.RAlgj3iMr1U5vHxJEtezGTrpawtn6JWHKunpIB8sdlLE8130_provenance.