@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is> .
@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/v3.0.0/void/> .
dgn-np:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_head {
   this: np:hasAssertion dgn-np:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_assertion ;
    np:hasProvenance dgn-np:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_provenance ;
    np:hasPublicationInfo dgn-np:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_provenance a np:Provenance .
  dgn-np:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_assertion {
   miriam-gene:89832 a ncit:C16612 .
  lld:C0025362 a ncit:C7057 .
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dgn-np:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_provenance {
   dgn-np:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_assertion dcterms:description "[In contrast to GTG banding, array CGH determined the exact number of deleted genes and thus allowed the identification of candidate genes for cleft palate (GREM1, CX36, MEIS2), congenital heart defect (ACTC, GREM1, CX36, MEIS2), and mental retardation (ARHGAP11A, CHRNA7, CHRM5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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  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:NP959904.RA0eulP4izQGYbv8r0f7LLRjL1jGwWQv2s_mgEVQcU4Is130_publicationInfo {
   this: dcterms:created "2015-08-25T14:47:26+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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