Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance.
- NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_assertion description "[Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance.
- NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_assertion evidence source_evidence_literature NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance.
- NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_assertion SIO_000772 16534102 NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance.
- NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_assertion wasDerivedFrom befree-2016 NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance.
- NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_assertion wasGeneratedBy ECO_0000203 NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance.
- befree-2016 importedOn "2016-02-19" NP539954.RAeKmrNAPX1GR9Dtv-bPxNY_tUPbxp0lYbQvl6RpqEGrk130_provenance.