Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance.
- NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_assertion description "[Other features noted in this kindred including epilepsy, cognitive impairment, depression, and migraine did not segregate with the HSP phenotype or mutation, and therefore the significance of these features to SPG4 is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance.
- NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_assertion evidence source_evidence_literature NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance.
- NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_assertion SIO_000772 15667412 NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance.
- NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_assertion wasDerivedFrom befree-2016 NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance.
- NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_assertion wasGeneratedBy ECO_0000203 NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance.
- befree-2016 importedOn "2016-02-19" NP477614.RAa8evJRcYP6U9h5BKYMxm3hrE2z0O5P7D8FWAGbkoRYM130_provenance.