Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance.
- NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_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." NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance.
- NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_assertion evidence source_evidence_literature NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance.
- NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_assertion SIO_000772 16574759 NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance.
- NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_assertion wasDerivedFrom gad-20150221 NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance.
- NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_assertion wasGeneratedBy ECO_0000203 NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP141136.RAMjZgxArM1GyY_e4OkRdkre57iNUV1_FGwBKA4yAABp4130_provenance.