Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance.
- NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_assertion description "[FOXC2 represents the second known gene to result in hereditary lymphedema, and LD is only the second hereditary disorder known to be caused by a mutation in a forkhead-family gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance.
- NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_assertion evidence source_evidence_literature NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance.
- NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_assertion SIO_000772 11078474 NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance.
- NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_assertion wasDerivedFrom befree-20140225 NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance.
- NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_assertion wasGeneratedBy ECO_0000203 NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP312102.RAdSnBRygdo8lA1ZgePsxfy7A0dNl1m4-H4NC52Es_dSM130_provenance.