Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance.
- NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_assertion description "[These findings suggest that the 20210A prothrombin allele represents an inherited risk factor for acute coronary syndrome among patients who have limited extent of coronary disease at angiography or who lack major metabolic and acquired risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance.
- NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_assertion evidence source_evidence_literature NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance.
- NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_assertion SIO_000772 11741359 NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance.
- NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_assertion wasDerivedFrom gad-20150221 NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance.
- NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_assertion wasGeneratedBy ECO_0000203 NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP72207.RAUiR4qvLgnqNNGkQLpGQ7dDkhbtdQ4l7lqc9CTUni9s4130_provenance.