Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance.
- NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_assertion description "[In our population, neither the factor V Leiden nor the G20210A prothrombin mutations are associated with fetal death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance.
- NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_assertion evidence source_evidence_literature NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance.
- NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_assertion SIO_000772 15948766 NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance.
- NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_assertion wasDerivedFrom gad-20130706 NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance.
- NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_assertion wasGeneratedBy ECO_0000203 NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance.
- gad-20130706 importedOn "2013-07-06" NP88234.RAh4cxfN5WEDxNBXwHaCvAblSw7zv_wk31RQfi6LcWVJs130_provenance.