@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_head {
  this: np:hasAssertion dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_assertion;
    np:hasProvenance dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_provenance;
    np:hasPublicationInfo dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_assertion a np:Assertion .
  
  dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_provenance a np:Provenance .
  
  dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_assertion {
  miriam-gene:6261 a ncit:C16612 .
  
  lld:C0151786 a ncit:C7057 .
  
  dgn-gda:DGNcb83f77ddb4cdacee485690e6643e3a4 sio:SIO_000628 miriam-gene:6261, lld:C0151786;
    a sio:SIO_001121 .
}

dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_provenance {
  dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_assertion dcterms:description
      "[Two fundamentally distinct cellular mechanisms (leaky channels and EC uncoupling) are proposed to explain how altered release channel function caused by different mutations in RyR1 could result in muscle weakness in CCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:11524458;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:28+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}