@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY> .
@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:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_head {
  this: np:hasAssertion dgn-np:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_assertion ;
    np:hasProvenance dgn-np:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_provenance ;
    np:hasPublicationInfo dgn-np:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_assertion a np:Assertion .
  dgn-np:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_provenance a np:Provenance .
  dgn-np:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_assertion {
  miriam-gene:5660 a ncit:C16612 .
  lld:C0149721 a ncit:C7057 .
  dgn-gda:DGN7a15a4afd5b8607ee5a2148cc003cdf0 sio:SIO_000628 miriam-gene:5660 , lld:C0149721 ;
    a sio:SIO_001121 .
}
dgn-np:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_provenance {
  dgn-np:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_assertion dcterms:description "[To test the hypothesis that carriers of Dutch founder mutations in cardiac myosin-binding protein C (MYBPC3), without left ventricular hypertrophy (LVH) or electrocardiographic abnormalities, have diastolic dysfunction on tissue Doppler imaging (TDI), which can be used for the screening of family members in the hypertrophic cardiomyopathy (HCM) population.]. 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:19356534 ;
    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:NP395245.RAZSqgUSm2WPL-n_XoCv2UkpEG_wYUxRE7ZSWtjmRJAAY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:55+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" .
}