Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance.
- NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_assertion description "[LAMP2 mutations may account for significant proportion of cases of hypertrophic cardiomyopathy children, especially when skeletal myopathy and/or Wolff-Parkinson-White syndrome is present/disease may be underrecognized in pediatric cardiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance.
- NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_assertion evidence source_evidence_literature NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance.
- NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_assertion SIO_000772 16144992 NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance.
- NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_assertion wasDerivedFrom lhgdn-20090331 NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance.
- NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_assertion wasGeneratedBy ECO_0000203 NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP134963.RAxGbdG1ENf_alihSDicC-6pJIfEIQP3o2DvDd6U2sglE130_provenance.