Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance.
- NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_assertion description "[A third PGRN sequence variation (R433W) was found in an FTD patient with family history of ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance.
- NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_assertion evidence source_evidence_literature NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance.
- NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_assertion SIO_000772 17202431 NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance.
- NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_assertion wasDerivedFrom befree-20140225 NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance.
- NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_assertion wasGeneratedBy ECO_0000203 NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP261473.RAv2qe1GUG7c82iPMnTf2CN40wgNlxXbVI05Hm5mxpusg130_provenance.