@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_head {
  this: np:hasAssertion dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_assertion;
    np:hasProvenance dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_provenance;
    np:hasPublicationInfo dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_assertion a np:Assertion .
  
  dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_provenance a np:Provenance .
  
  dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_assertion {
  miriam-gene:6722 a ncit:C16612 .
  
  lld:C0025958 a ncit:C7057 .
  
  dgn-gda:DGNd68848bb87056cf4d79bae4ac102ad1d sio:SIO_000628 miriam-gene:6722, lld:C0025958;
    a sio:SIO_001121 .
}

dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_provenance {
  dgn-np:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_assertion dcterms:description
      "[While disruption of the MKL2:SRF axis has been associated with severe microcephaly and disordered brain development in multiple model systems, the role of this transcription factor complex has not been previously demonstrated in human brain development.]. 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:23692340;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1079374.RApYQnt6wDdOHGzCjhalwaSgZCAWQad-LHRNEP91XK0X8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:55+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}