Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance.
- NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_assertion description "[All eleven RyR2 mutations cluster into 3 regions of RyR2 that are homologous to the three malignant hyperthermia (MH)/central core disease (CCD) mutation regions of the skeletal muscle ryanodine receptor/calcium release channel RyR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance.
- NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_assertion evidence source_evidence_literature NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance.
- NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_assertion SIO_000772 11807805 NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance.
- NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_assertion wasDerivedFrom befree-2016 NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance.
- NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_assertion wasGeneratedBy ECO_0000203 NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance.
- befree-2016 importedOn "2016-02-19" NP343003.RADewOGW5Rv5V65HsdfemE15A4ivwvA1syCYZKf483pZk130_provenance.