Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.
- NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_assertion description "[hypertrophic cardiomyopathy, left ventricular non-compaction (HCM and LVNC) may appear as overlapping entities/ACTC E101K mutation should be considered in the genetic diagnosis of LVNC, apical HCM, and septal defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.
- NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_assertion evidence source_evidence_literature NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.
- NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_assertion SIO_000772 17611253 NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.
- NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_assertion wasDerivedFrom lhgdn-20090331 NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.
- NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_assertion wasGeneratedBy ECO_0000203 NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.