@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k> .
@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:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_head {
  this: np:hasAssertion dgn-np:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_assertion;
    np:hasProvenance dgn-np:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_provenance;
    np:hasPublicationInfo dgn-np:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_assertion a np:Assertion .
  
  dgn-np:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_provenance a np:Provenance .
  
  dgn-np:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_assertion {
  miriam-gene:10993 a ncit:C16612 .
  
  lld:C0282666 a ncit:C7057 .
  
  dgn-gda:DGN139ce46ac20525deb1249c6e7669ac9a sio:SIO_000628 miriam-gene:10993, lld:C0282666;
    a sio:SIO_001121 .
}

dgn-np:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_provenance {
  dgn-np:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_assertion dcterms:description
      "[We performed routine karyotyping, IGF2 gene sequencing and investigated DNA methylation of the IGF2 differentially methylated region (DMR)0 and H19 DMR using pyrosequencing, in four women selected for very low birth weight (<-3 SDS for gestational age), precocious pubarche, short adult stature (<-2 SDS), and insulin resistance (defined as HOMA-IS < 80%); and compared their methylation results to those of 95 control subjects.]. 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:22646060;
    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:NP682405.RALUN09GIDO1cx3NRELp0808tBeaWM6pkvx1kv20Red_k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:54+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" .
}