Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance.
- NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_assertion description "[A common polymorphism in the gene for factor XIII A subunit (F13A1 V34L) has been associated with a decreased risk for coronary artery disease, cerebrovascular disease, and deep venous thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance.
- NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_assertion evidence source_evidence_literature NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance.
- NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_assertion SIO_000772 11941274 NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance.
- NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_assertion wasDerivedFrom lhgdn-20090331 NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance.
- NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_assertion wasGeneratedBy ECO_0000203 NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP141477.RAGk8hYd8F1R060LZbEK3EY74lp-0E6_SNofgBy0VHl40130_provenance.