@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso> .
@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:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_head {
   this: np:hasAssertion dgn-np:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_assertion ;
    np:hasProvenance dgn-np:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_provenance ;
    np:hasPublicationInfo dgn-np:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_assertion a np:Assertion .
  dgn-np:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_provenance a np:Provenance .
  dgn-np:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_assertion {
   miriam-gene:2137 a ncit:C16612 .
  lld:C0015306 a ncit:C7057 .
  dgn-gda:DGN8ce0cd7da16b0388e3ecb5229f5cad9d sio:SIO_000628 miriam-gene:2137 , lld:C0015306 ;
    a sio:SIO_001121 .
}
dgn-np:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_provenance {
   dgn-np:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_assertion dcterms:description "[Based on PCR-assisted analyses of both a human/rodent mono-chromosomal hybrid cell panel and a radiation hybrid mapping panel, EXTR1 was localized to the chromosome 8p21 region, where loss of heterozygosity has been frequently observed in various tumors, and EXTR2 was assigned to the chromosome 1p21 region, where osteopetrosis, a dominant hereditary disease of bone, has been mapped by genetic linkage analysis, implying that the protein products of these two EXT-related genes, as well as of the EXT genes, have potential tumor suppressor activity.]. 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:9473480 ;
    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:NP637100.RAV8KKvQuNb4wXGeAZS5OlgoLikiZgRSY6tAjUPC3Mhso130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:24+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" .
}