Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion description "[Hereditary hypofibrinolysis, which is mediated by 4G/4G homozygosity for the PAI-1 gene, is an independent risk factor for pregnancy complications, probably acting through thrombotic induction of placental insufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion evidence source_evidence_literature NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion SIO_000772 25723084 NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion wasDerivedFrom befree-2016 NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_assertion wasGeneratedBy ECO_0000203 NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266728.RApXkNfoOP5hYZjU2EGB42xveiRtnAySlkHr84RjpEd2s130_provenance.