Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance.
- NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_assertion description "[The teenage sister of the proband is a carrier of the same LAMP2 mutation and has HCM without skeletal myopathy or WPW.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance.
- NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_assertion evidence source_evidence_literature NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance.
- NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_assertion SIO_000772 16144992 NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance.
- NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_assertion wasDerivedFrom befree-2016 NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance.
- NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_assertion wasGeneratedBy ECO_0000203 NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance.
- befree-2016 importedOn "2016-02-19" NP512336.RA2fcI-SKxGBUNmURtPLo0k8W51ixKETq2BVjP_cwd8Jk130_provenance.