Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance.
- NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_assertion description "[Pathogenetic mechanisms of RYR1-related MmD are currently not well understood, but likely to involve altered excitability and/or changes in calcium homeoestasis; calcium-binding motifs within the selenoprotein N protein also suggest a possible role in calcium handling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance.
- NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_assertion evidence source_evidence_literature NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance.
- NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_assertion SIO_000772 17631035 NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance.
- NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_assertion wasDerivedFrom befree-2016 NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance.
- NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_assertion wasGeneratedBy ECO_0000203 NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance.
- befree-2016 importedOn "2016-02-19" NP620068.RAISu6r8VWDOk7QB18V_wHygumaKYyPgztAasyLPWEiJc130_provenance.