Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance.
- NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_assertion description "[Previous reports have shown linkage of hereditary motor and sensory neuropathy, type I (HMSN I), a dominantly inherited hypertrophic neuropathy, to the locus for the Duffy blood group on the long arm of chromosome 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance.
- NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_assertion evidence source_evidence_literature NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance.
- NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_assertion SIO_000772 6865476 NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance.
- NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_assertion wasDerivedFrom befree-20140225 NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance.
- NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_assertion wasGeneratedBy ECO_0000203 NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP794802.RAwXy2AMeHE4WelLHFBFOUipEnpsaRj388GXFfzgfbVP8130_provenance.