Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance.
- NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_assertion description "[Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance.
- NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_assertion evidence source_evidence_literature NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance.
- NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_assertion SIO_000772 20215591 NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance.
- NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_assertion wasDerivedFrom befree-20150227 NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance.
- NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_assertion wasGeneratedBy ECO_0000203 NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748654.RAyMnEfHrensEIg6RyJUD-HukD91a1tpVHmTS1MOZefOQ130_provenance.