Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance.
- NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_assertion wasGeneratedBy ECO_0000203 NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance.
- NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_assertion wasDerivedFrom befree-20140225 NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance.
- NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_assertion SIO_000772 17054105 NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance.
- NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_assertion evidence source_evidence_literature NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance.
- NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_assertion description "[A de novo heterozygous HRAS change was detected in all the subjects diagnosed with CS, while no lesion was observed with any of the other phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297540.RA6p_L2taUK8DSHrJXooPU-z4F6Jg69A4X8TYa00BZafg130_provenance.