@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0> .
@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:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_head {
   this: np:hasAssertion dgn-np:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_assertion ;
    np:hasProvenance dgn-np:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_provenance ;
    np:hasPublicationInfo dgn-np:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_assertion a np:Assertion .
  dgn-np:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_provenance a np:Provenance .
  dgn-np:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_assertion {
   miriam-gene:54741 a ncit:C16612 .
  lld:C0011847 a ncit:C7057 .
  dgn-gda:DGN6d81a0eaed89cc0c08c4054d59b2e559 sio:SIO_000628 miriam-gene:54741 , lld:C0011847 ;
    a sio:SIO_001121 .
}
dgn-np:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_provenance {
   dgn-np:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_assertion dcterms:description "[As part of an effort to identify informative molecular markers for genetic analysis of human pedigrees segregating for obesity, we have developed a genetic map of human 1p in the region of the OB receptor (OBR), the gene that is defective in murine diabetes (Obrdb) and rat Zucker fatty (Obrfa) mutations located on mid-chromosome 4 and chromosome 5, respectively.]. 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:8743992 ;
    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:NP701812.RADHHIY4sUMO2qtBmkjJH5zaL2MoIHwogmoMMJb4WOxU0130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:06+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" .
}