Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance.
- NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_assertion description "[The frequency of either the FVL or prothrombin sequence variant was not increased in idiopathic PE patients compared with nonidiopathic PE patients or patients who had PE excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance.
- NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_assertion evidence source_evidence_literature NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance.
- NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_assertion SIO_000772 16574759 NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance.
- NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_assertion wasDerivedFrom gad-20150221 NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance.
- NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_assertion wasGeneratedBy ECO_0000203 NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP108505.RAe0C37v9AQCdVqpOeKYZsBiDFvPFC0X9UxRAPB4M3Xh0130_provenance.