@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c> .
@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:NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c130_head {
  this: np:hasAssertion dgn-np:NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c130_assertion ;
    np:hasProvenance dgn-np:NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c130_provenance ;
    np:hasPublicationInfo dgn-np:NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c130_provenance a np:Provenance .
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}
dgn-np:NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c130_assertion {
  miriam-gene:1436 a ncit:C16612 .
  lld:C0027651 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c130_provenance {
  dgn-np:NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c130_assertion dcterms:description "[To investigate whether inflammatory disease or neoplasia was the dominant consequence of autocrine regulation by CSF-1 in CSF-1 receptor (CSF-1R)-expressing cells, we created mice that express CSF-1 under the control of the CSF-1R promoter/first intron driver [transgene TgN(Csf1r-Csf1)Ers (TgRC) mice], which have reduced thymic size, a short lifetime, and low body weight and develop osteoporosis.]. 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-20140225 ;
    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:NP848508.RA-gkA9bXoFzmZLUCh5R2np5AO-QqaDiGo4qoAxl0SK8c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:38+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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