Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance.
- NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_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." NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance.
- NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_assertion evidence source_evidence_literature NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance.
- NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_assertion SIO_000772 16144992 NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance.
- NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_assertion wasDerivedFrom lhgdn-20090331 NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance.
- NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_assertion wasGeneratedBy ECO_0000203 NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198120.RA86jZ6SlGzPdCa47ca8tpCsmrKve319uC_wDr_84lUMU130_provenance.