@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk> .
@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:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_head {
  this: np:hasAssertion dgn-np:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_assertion;
    np:hasProvenance dgn-np:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_provenance;
    np:hasPublicationInfo dgn-np:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_assertion a np:Assertion .
  
  dgn-np:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_provenance a np:Provenance .
  
  dgn-np:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_assertion {
  miriam-gene:90226 a ncit:C16612 .
  
  lld:C0079541 a ncit:C7057 .
  
  dgn-gda:DGN651253bed2411d8b677ae45e2cc0f5a8 sio:SIO_000628 miriam-gene:90226, lld:C0079541;
    a sio:SIO_001121 .
}

dgn-np:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_provenance {
  dgn-np:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_assertion dcterms:description
      "[The main difference between the mutation positive SRP type II group and the mutation negative SRP type II group was the presence of holoprosencephaly and polymycrogyria in the mutation negative group.]. 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:22499340;
    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:NP307112.RA6dHOA9aFbVgi3m6OPKjK_AubOTwNzh8CQE9tWKAh7Yk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+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" .
}