@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo> .
@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:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_head {
  this: np:hasAssertion dgn-np:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_assertion;
    np:hasProvenance dgn-np:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_provenance;
    np:hasPublicationInfo dgn-np:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_assertion a np:Assertion .
  
  dgn-np:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_provenance a np:Provenance .
  
  dgn-np:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_assertion {
  miriam-gene:58478 a ncit:C16612 .
  
  lld:C0037772 a ncit:C7057 .
  
  dgn-gda:DGN72c7df273f149032d827364b87c7c3ab sio:SIO_000628 miriam-gene:58478, lld:C0037772;
    a sio:SIO_001121 .
}

dgn-np:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_provenance {
  dgn-np:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_assertion dcterms:description
      "[X-linked hydrocephalus, HSAS (hydrocephalus due to stenosis of aqueduct of Sylvius), MASA (mental retardation, aphasia, shuffling gait, and adducted thumbs), and CRASH (corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraplegia, and hydrocephalus) syndromes are allelic disorders.]. 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:15662685;
    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:NP494778.RAALJj78iRt1kCZCnnFD6Hmf_le2QkYw7xceGdr-qtvjo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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" .
}