Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance.
- NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_assertion description "[We identified a male Polish patient with a very rare minor homozygous GG genotype of the tissue factor (TF) +5466A>G polymorphism, who within two months experienced a transient ischemic attack (TIA) and ischemic stroke of unknown origin associated with the presence of patent foramen ovale below 40 years of age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance.
- NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_assertion evidence source_evidence_literature NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance.
- NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_assertion SIO_000772 19203804 NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance.
- NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_assertion wasDerivedFrom befree-2016 NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance.
- NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_assertion wasGeneratedBy ECO_0000203 NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance.
- befree-2016 importedOn "2016-02-19" NP719423.RAyJLQrY8hlnFTvLM06o5qAwVM1vGsH9Ys0Hza6LejtQM130_provenance.