Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance.
- NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_assertion description "[Dysregulation of calcium signals because of defects of the skeletal muscle sarcoplasmic reticulum calcium release channel (ryanodine receptor; RyR1) is causative of several congenital muscle disorders including malignant hyperthermia (MH; MIM #145600), central core disease (CCD; MIM #11700), specific forms of multi-minicore disease (MmD; MIM # 255320) and centronuclear myopathy (CNM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance.
- NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_assertion evidence source_evidence_literature NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance.
- NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_assertion SIO_000772 18313359 NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance.
- NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_assertion wasDerivedFrom befree-2016 NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance.
- NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_assertion wasGeneratedBy ECO_0000203 NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance.
- befree-2016 importedOn "2016-02-19" NP658306.RAU7vvBcLoWmBlAdDIDK_On6APHI7V19PeIC_Hl0jMVTE130_provenance.