Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance.
- NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_assertion description "[We now show that point mutations in the cytoplasmic domain that modify a PKC target motif (RSTK) or an adjacent serine residue abolish P0 adhesion function and can cause peripheral neuropathy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance.
- NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_assertion evidence source_evidence_literature NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance.
- NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_assertion SIO_000772 11673479 NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance.
- NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_assertion wasDerivedFrom befree-20140225 NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance.
- NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_assertion wasGeneratedBy ECO_0000203 NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance.
- befree-20140225 importedOn "2014-02-25" NP201917.RA2ML8WAx3Sg62ObjLjFNiIOelw6waOaHFfzPSPeG2K50130_provenance.