Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance.
- NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_assertion description "[High prevalence of inherited prothrombotic risk factors in 134 consecutive patients with von Willebrand disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance.
- NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_assertion evidence source_evidence_literature NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance.
- NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_assertion SIO_000772 16680739 NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance.
- NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_assertion wasDerivedFrom gad-20150221 NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance.
- NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_assertion wasGeneratedBy ECO_0000203 NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP108269.RABh3j65PNsLP7HmgLyJwEKiS9-yfxDih0RcxZpIEMqDE130_provenance.