Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.
- NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_assertion description "[Because mutations in the COQ2 gene are associated with severe inherited myopathy, we hypothesized that common, mild genetic variation in COQ2 would be associated with inter-individual variation in statin intolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.
- NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_assertion evidence source_evidence_literature NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.
- NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_assertion SIO_000772 17376224 NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.
- NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_assertion wasDerivedFrom befree-20140225 NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.
- NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_assertion wasGeneratedBy ECO_0000203 NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.