Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance.
- NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_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." NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance.
- NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_assertion evidence source_evidence_literature NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance.
- NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_assertion SIO_000772 11872951 NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance.
- NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_assertion wasDerivedFrom befree-2016 NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance.
- NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_assertion wasGeneratedBy ECO_0000203 NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance.
- befree-2016 importedOn "2016-02-19" NP346941.RA0-A6JFeX62nN0ld0gZ0AEakr6tXcbAdBo0eHRUqQpfY130_provenance.