Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance.
- NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_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." NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance.
- NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_assertion evidence source_evidence_literature NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance.
- NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_assertion SIO_000772 16574759 NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance.
- NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_assertion wasDerivedFrom befree-2016 NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance.
- NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_assertion wasGeneratedBy ECO_0000203 NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance.
- befree-2016 importedOn "2016-02-19" NP542707.RAOnpCqX5ubr3DFK9S0vTby2K2uL34ngY2ffrYzT3yDlg130_provenance.