Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance.
- NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_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." NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance.
- NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_assertion evidence source_evidence_literature NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance.
- NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_assertion SIO_000772 11872951 NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance.
- NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_assertion wasDerivedFrom gad-20150221 NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance.
- NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_assertion wasGeneratedBy ECO_0000203 NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP52802.RAbf7MhPKGqwqZrhNNNulFKAdd7-tlmfceFZkJlUqDIRg130_provenance.