@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI> .
@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:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_head {
   this: np:hasAssertion dgn-np:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_assertion ;
    np:hasProvenance dgn-np:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_provenance ;
    np:hasPublicationInfo dgn-np:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_assertion a np:Assertion .
  dgn-np:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_provenance a np:Provenance .
  dgn-np:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_assertion {
   miriam-gene:632 a ncit:C16612 .
  lld:C0175699 a ncit:C7057 .
  dgn-gda:DGN35a2883102f9cffc85403e29f47625ba sio:SIO_000628 miriam-gene:632 , lld:C0175699 ;
    a sio:SIO_001122 .
}
dgn-np:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_provenance {
   dgn-np:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_assertion dcterms:description "[Cranial osteoblasts from an SCS patient with a Y103X mutation inducing deletion of the Twist bHLH domain showed decreased Fgfr2 mRNA levels associated with decreased expression of Runx2, bone sialoprotein (BSP) and osteocalcin (OC), markers of differentiated osteoblasts, compared with wild-type osteoblasts.]. 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:15829502 ;
    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:NP267387.RAl7BOOywylw4Xk50x5oEl9F4_z1nmEJmCPLLcdL0bNXI130_publicationInfo {
   this: dcterms:created "2015-08-25T14:40:12+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" .
}