@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_head {
  this: np:hasAssertion dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_assertion;
    np:hasProvenance dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_provenance;
    np:hasPublicationInfo dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_assertion a np:Assertion .
  
  dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_provenance a np:Provenance .
  
  dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_assertion {
  miriam-gene:1769 a ncit:C16612 .
  
  lld:C0007194 a ncit:C7057 .
  
  dgn-gda:DGNb419d752b060d4afde4f49e0824edfba sio:SIO_000628 miriam-gene:1769, lld:C0007194;
    a sio:SIO_001121 .
}

dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_provenance {
  dgn-np:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_assertion dcterms:description
      "[The inability of the five cTnI mutations investigated to fully inhibit ATPase activity/force development and the generally larger increases in Ca2+ sensitivity than observed for most hypertrophic cardiomyopathy mutations would likely lead to severe diastolic dysfunction and may be the major physiological factors responsible for causing the restrictive cardiomyopathy phenotype in some of the genetically affected individuals.]. 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:15961398;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP356190.RAle1nuy9oqlgGiG74rNjtTvRHQUe_Mhtu7QJcDSzK1S0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:05+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}