@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk> .
@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:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_head {
  this: np:hasAssertion dgn-np:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_assertion;
    np:hasProvenance dgn-np:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_provenance;
    np:hasPublicationInfo dgn-np:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_assertion a np:Assertion .
  
  dgn-np:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_provenance a np:Provenance .
  
  dgn-np:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_assertion {
  miriam-gene:1125 a ncit:C16612 .
  
  lld:C0349204 a ncit:C7057 .
  
  dgn-gda:DGNb6cf833fea92dfc891a023cd07377853 sio:SIO_000628 miriam-gene:1125, lld:C0349204;
    a sio:SIO_001121 .
}

dgn-np:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_provenance {
  dgn-np:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_assertion dcterms:description
      "[Risk for psychosis can be assessed on the basis of genetic risk, referred to in the literature as family high risk (FHR) or through the presence of clinical high risk symptoms (CHR).]. 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:23611242;
    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:NP854559.RA7ZkZyBqg4ohZdUB9c5rOxx30yfcIsyiAChddjABs1rk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:42+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" .
}