@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_head {
  this: np:hasAssertion dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_assertion;
    np:hasProvenance dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_provenance;
    np:hasPublicationInfo dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_assertion a np:Assertion .
  
  dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_provenance a np:Provenance .
  
  dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_assertion {
  miriam-gene:8431 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGN383aedb97671500c33d53c0b31607dc7 sio:SIO_000628 miriam-gene:8431, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_provenance {
  dgn-np:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_assertion dcterms:description
      "[There was no association with corrected birth weight in 382 normal babies, but the only AA baby was 4,069 g. Our study suggests that genetic variation in SHP is unlikely to be common in the predisposition to diabetes, obesity, or increased birth weight in U.K. Caucasians.]. 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:12716764;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP795861.RAKyrniegWCmCtgF6_X8N-HoXGCd1kyURBml9YMFwyhik130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:41+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}