Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance.
- NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_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." NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance.
- NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_assertion evidence source_evidence_literature NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance.
- NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_assertion SIO_000772 16680739 NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance.
- NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_assertion wasDerivedFrom gad-20150221 NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance.
- NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_assertion wasGeneratedBy ECO_0000203 NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance.
- gad-20150221 importedOn "2015-02-21" NP100471.RAHC19B_XuDcMmqLJNDOiPYm6zkVbsh__00PcC3eWVl5U130_provenance.