Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.
- NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_assertion description "[We report a rare case of double heterozygous type I protein C deficiency and factor V Leiden in a patient with classic myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.
- NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_assertion evidence source_evidence_literature NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.
- NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_assertion SIO_000772 10726006 NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.
- NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_assertion wasDerivedFrom befree-20140225 NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.
- NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_assertion wasGeneratedBy ECO_0000203 NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.