@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4> .
@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:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_head {
  this: np:hasAssertion dgn-np:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_assertion ;
    np:hasProvenance dgn-np:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_provenance ;
    np:hasPublicationInfo dgn-np:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_assertion a np:Assertion .
  dgn-np:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_provenance a np:Provenance .
  dgn-np:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_assertion {
  miriam-gene:10660 a ncit:C16612 .
  lld:C0027765 a ncit:C7057 .
  dgn-gda:DGN89b8bb341fa74709e1f445a41c272337 sio:SIO_000628 miriam-gene:10660 , lld:C0027765 ;
    a sio:SIO_001121 .
}
dgn-np:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_provenance {
  dgn-np:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_assertion dcterms:description "[The number of homeobox genes currently linked to human nervous system disease is surprisingly low, perhaps reflecting the essential functions of these genes throughout embryogenesis or the degree of functional redundancy during central nervous system 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:18241223 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP850077.RAICppZCvLgqhgpWEyXAbYOg-JKLFN-Af0hMhjo6JooV4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:16+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}