Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance.
- NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_assertion description "[In the present study, we screened for protein C amidolytic activity in patients admitted to the National Cardiovascular Center Hospital, and we identified among them 43 probands and 51 relatives with heterozygous protein C deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance.
- NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_assertion evidence source_evidence_literature NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance.
- NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_assertion SIO_000772 10230891 NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance.
- NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_assertion wasDerivedFrom befree-2016 NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance.
- NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_assertion wasGeneratedBy ECO_0000203 NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance.
- befree-2016 importedOn "2016-02-19" NP251823.RAg9Iic-td0siOGxSmUxqmC2lgwV4Snwh2TXaPeRe3UOk130_provenance.