@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0> .
@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:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_head {
  this: np:hasAssertion dgn-np:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_assertion;
    np:hasProvenance dgn-np:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_provenance;
    np:hasPublicationInfo dgn-np:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_assertion a np:Assertion .
  
  dgn-np:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_provenance a np:Provenance .
  
  dgn-np:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_assertion {
  miriam-gene:3479 a ncit:C16612 .
  
  lld:C0271563 a ncit:C7057 .
  
  dgn-gda:DGNf3d8e39b5de4e9409c96c40c1f0f7f00 sio:SIO_000628 miriam-gene:3479, lld:C0271563;
    a sio:SIO_001121 .
}

dgn-np:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_provenance {
  dgn-np:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_assertion dcterms:description
      "[The phenotypic characteristics of isolated growth hormone deficiency (IGHD) type IB in humans, such as autosomal recessive inheritance, time of onset of growth retardation, diminished secretion of growth hormone (GH) and IGF-I, proportional reduction in weight and size, and delay in sexual maturation, has much in common with the phenotype of the homozygous little/little (lit/lit) mouse.]. 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:8618801;
    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:NP154900.RAaozwh6VRdFc9WNQUW27iACPzsYKepq4jf1mwSSkNoL0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}