Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance.
- NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_assertion description "[Increased frequency of the C3*F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance.
- NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_assertion evidence source_evidence_literature NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance.
- NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_assertion SIO_000772 11872951 NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance.
- NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_assertion wasDerivedFrom befree-20150227 NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance.
- NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_assertion wasGeneratedBy ECO_0000203 NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP391322.RAcsfG0ZtLQLVYOWF6CM7oeYfbPkFAT8sos7c8tXiQnjE130_provenance.