@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg> .
@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:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_head {
  this: np:hasAssertion dgn-np:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_assertion;
    np:hasProvenance dgn-np:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_provenance;
    np:hasPublicationInfo dgn-np:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_assertion a np:Assertion .
  
  dgn-np:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_provenance a np:Provenance .
  
  dgn-np:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_assertion {
  miriam-gene:1277 a ncit:C16612 .
  
  lld:C0009326 a ncit:C7057 .
  
  dgn-gda:DGN4a4fdda8256397598e2440f833cfe50d sio:SIO_000628 miriam-gene:1277, lld:C0009326;
    a sio:SIO_001121 .
}

dgn-np:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_provenance {
  dgn-np:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_assertion dcterms:description
      "[Two COL1A1 and two COL1A2 RFLPs were more polymorphic than in the English population, making them better markers for the analysis of Italian families affected by osteogenesis imperfecta and some other inherited collagen diseases.]. 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:2572536;
    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:NP838069.RA043Q_y9jgCUptWOHkKOOUPZe1VsN7WNljHVn0fHsGXg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:32+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" .
}