@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg> .
@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:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_head {
  this: np:hasAssertion dgn-np:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_assertion;
    np:hasProvenance dgn-np:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_provenance;
    np:hasPublicationInfo dgn-np:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_assertion a np:Assertion .
  
  dgn-np:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_provenance a np:Provenance .
  
  dgn-np:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_assertion {
  miriam-gene:64175 a ncit:C16612 .
  
  lld:C1458156 a ncit:C7057 .
  
  dgn-gda:DGN71a079d9526b3f041396aacd4060f08a sio:SIO_000628 miriam-gene:64175, lld:C1458156;
    a sio:SIO_001121 .
}

dgn-np:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_provenance {
  dgn-np:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_assertion dcterms:description
      "[These results expand the range of CRTAP/LEPRE1 mutations that result in recessive OI and emphasize the importance of distinguishing recurrence of severe OI of recessive inheritance from those that result from parental germline mosaicism for COL1A1 or COL1A2 mutations.]. 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:18566967;
    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:NP800856.RA0Js9vHxulMMllarIGisaFW8u235XkKyhMiiBJbapCPg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:11+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" .
}