@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE> .
@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:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_head {
  this: np:hasAssertion dgn-np:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_assertion;
    np:hasProvenance dgn-np:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_provenance;
    np:hasPublicationInfo dgn-np:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_assertion a np:Assertion .
  
  dgn-np:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_provenance a np:Provenance .
  
  dgn-np:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_assertion {
  miriam-gene:4625 a ncit:C16612 .
  
  lld:C0745103 a ncit:C7057 .
  
  dgn-gda:DGN997809dd5ccb03f840c4de72bbe8138f sio:SIO_000628 miriam-gene:4625, lld:C0745103;
    a sio:SIO_001121 .
}

dgn-np:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_provenance {
  dgn-np:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_assertion dcterms:description
      "[Several mutations within the gene coding for the cardiac beta myosin heavy chain (designed MYH7) have been shown to be responsible for Familial Hypertrophic Cardiomyopathy (FHC) in several families, and evidence of genetic heterogeneity has been reported.]. 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:7815466;
    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:NP597281.RAbRtIBdhX_Jp4ugyA-_mm3lKhRCFk-1qGN5LfmLgz-uE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:59+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" .
}