Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_assertion type Assertion NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_head.
- NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_assertion description "[Mutations in troponin T (TNNT2) gene represent the important part of currently identified disease-causing mutations in hypertrophic (HCM) and dilated (DCM) cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_provenance.
- NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_assertion evidence source_evidence_literature NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_provenance.
- NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_assertion SIO_000772 22292720 NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_provenance.
- NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_assertion wasDerivedFrom befree-20140225 NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_provenance.
- NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_assertion wasGeneratedBy ECO_0000203 NP690139.RAIeVfMgOChcmnnIPuIEmojOv7Nu3e3U2PLk2e7kBDACM130_provenance.