@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w> .
@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:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_head {
  this: np:hasAssertion dgn-np:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_assertion;
    np:hasProvenance dgn-np:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_provenance;
    np:hasPublicationInfo dgn-np:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_assertion a np:Assertion .
  
  dgn-np:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_provenance a np:Provenance .
  
  dgn-np:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_assertion {
  miriam-gene:3479 a ncit:C16612 .
  
  lld:C0015544 a ncit:C7057 .
  
  dgn-gda:DGN89611a3369c27f719e6c8eb3c3dc0c6b sio:SIO_000628 miriam-gene:3479, lld:C0015544;
    a sio:SIO_001121 .
}

dgn-np:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_provenance {
  dgn-np:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_assertion dcterms:description
      "[The importance of IGF-I for both in utero as well as postnatal human growth is highlighted by rare human homozygous IGF1 mutations, which are characterized by intrauterine growth retardation (IUGR), microcephaly, mental retardation and severe postnatal growth failure.]. 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:23502138;
    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:NP275737.RAp5kdayY5_oI21c2jxQLFWnEf1cUkanIdMOLYoLGrd2w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:35+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" .
}