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- source_evidence_literature type ECO_0000212 NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.
- NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_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." NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.
- NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_assertion evidence source_evidence_literature NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.
- NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_assertion SIO_000772 17376224 NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.
- NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_assertion wasDerivedFrom befree-2016 NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.
- NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_assertion wasGeneratedBy ECO_0000203 NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.
- befree-2016 importedOn "2016-02-19" NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.