Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance.
- NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_assertion description "[To assess first-pass magnetic resonance (MR) imaging in the evaluation of perfusion impairment in a genetically homogeneous population of patients with hypertrophic cardiomyopathy (HCM) and the Asp175Asn mutation of the alpha-tropomyosin gene and to evaluate the association between hypertrophy and perfusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance.
- NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_assertion evidence source_evidence_literature NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance.
- NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_assertion SIO_000772 12511681 NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance.
- NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_assertion wasDerivedFrom befree-2016 NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance.
- NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_assertion wasGeneratedBy ECO_0000203 NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance.
- befree-2016 importedOn "2016-02-19" NP379333.RAOogXKecGMsqsGs4hZatTETGIXicgFsLLZ3QqzGVKc7A130_provenance.