Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance.
- NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_assertion description "[Furthermore, combinations of PT-20210A or FVL with PAI-1 (4G/4G) were significantly more frequent in APS patients (5.8%) than in normal controls (0.5%, p=0.016).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance.
- NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_assertion evidence source_evidence_literature NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance.
- NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_assertion SIO_000772 11454529 NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance.
- NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_assertion wasDerivedFrom befree-20140225 NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance.
- NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_assertion wasGeneratedBy ECO_0000203 NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP598853.RAtXJdJx-0oQaakf9dEqs47tFpC-e8SYkPJLzIYHl33qA130_provenance.