@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8> .
@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:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_head {
  this: np:hasAssertion dgn-np:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_assertion ;
    np:hasProvenance dgn-np:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_provenance ;
    np:hasPublicationInfo dgn-np:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_assertion a np:Assertion .
  dgn-np:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_provenance a np:Provenance .
  dgn-np:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_assertion {
  miriam-gene:4880 a ncit:C16612 .
  lld:C0343284 a ncit:C7057 .
  dgn-gda:DGNc78595a35027b1bd1ffa4509389030b4 sio:SIO_000628 miriam-gene:4880 , lld:C0343284 ;
    a sio:SIO_001121 .
}
dgn-np:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_provenance {
  dgn-np:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_assertion dcterms:description "[To elucidate whether systemic administration of CNP would be a novel medical treatment for chondrodysplasias, for which no drug therapy has yet been developed, we investigated the effect of circulating CNP by using the CNP transgenic mice with an increased circulating CNP under the control of human serum amyloid P component promoter (SAP-Nppc-Tg mice).]. 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:20610569 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP699899.RATxZm2nWUyBae1V8qA8UPiWsz155_JTKoAxaJC7zVLR8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:05+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:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}