@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY> .
@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:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_head {
  this: np:hasAssertion dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_assertion;
    np:hasProvenance dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_provenance;
    np:hasPublicationInfo dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_assertion a np:Assertion .
  
  dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_provenance a np:Provenance .
  
  dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_assertion {
  miriam-gene:85358 a ncit:C16612 .
  
  lld:C1849930 a ncit:C7057 .
  
  dgn-gda:DGNb7a1769460664294e102f89c742ebb9b sio:SIO_000628 miriam-gene:85358, lld:C1849930;
    a sio:SIO_001121 .
}

dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_provenance {
  dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_assertion dcterms:description
      "[Although SHANK3 is considered to be the most likely candidate gene for the neurological abnormalities in PMDS patients, the cellular and molecular phenotypes associated with this syndrome in human neurons are unknown.]. 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:24132240;
    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:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}