@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI> .
@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:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_head {
  this: np:hasAssertion dgn-np:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_assertion;
    np:hasProvenance dgn-np:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_provenance;
    np:hasPublicationInfo dgn-np:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_assertion a np:Assertion .
  
  dgn-np:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_provenance a np:Provenance .
  
  dgn-np:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_assertion {
  miriam-gene:1403 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGN4cdda117495028e9875328318154179b sio:SIO_000628 miriam-gene:1403, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_provenance {
  dgn-np:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_assertion dcterms:description
      "[Crouzon syndrome, one of the best known of many craniofacial syndromes, is an autosomal dominant disorder characterized by craniosynostosis, prominent eyes, and midfacial hypoplasia due to abnormal development and premature fusion of the skull.]. 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:8650126;
    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:NP680825.RAkvBAaUbG2g-O-FRobhCW4fppSgn6rQLGY58B-0LcfTI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:50+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" .
}