@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM> .
@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:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_head {
  this: np:hasAssertion dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_assertion;
    np:hasProvenance dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_provenance;
    np:hasPublicationInfo dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_assertion a np:Assertion .
  
  dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_provenance a np:Provenance .
  
  dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_assertion {
  miriam-gene:7139 a ncit:C16612 .
  
  lld:C1449563 a ncit:C7057 .
  
  dgn-gda:DGN31d8356918f45a8469f364ce1d6e76bc sio:SIO_000628 miriam-gene:7139, lld:C1449563;
    a sio:SIO_001121 .
}

dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_provenance {
  dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_assertion dcterms:description
      "[Known candidate loci for isolated conduction disorders, isolated DCM and conduction disorders complicated by DCM were excluded from disease causation in this family by linkage analysis, with the exception of the DCM-associated (CMD1D) locus on chromosome 1q32, where a maximum multipoint lod score of 3.7 in the interval between D1S3753 and D1S414, was generated.]. 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:16086176;
    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:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:51+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" .
}