@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U> .
@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:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_head {
   this: np:hasAssertion dgn-np:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_assertion ;
    np:hasProvenance dgn-np:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_provenance ;
    np:hasPublicationInfo dgn-np:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_assertion a np:Assertion .
  dgn-np:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_provenance a np:Provenance .
  dgn-np:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_assertion {
   miriam-gene:8030 a ncit:C16612 .
  lld:C0008626 a ncit:C7057 .
  dgn-gda:DGNae42b2036ea8b23c20915904aa0c024d sio:SIO_000628 miriam-gene:8030 , lld:C0008626 ;
    a sio:SIO_001121 .
}
dgn-np:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_provenance {
   dgn-np:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_assertion dcterms:description "[Moreover, the pattern of chromosomal aberrations (gains at chromosome arms 2q, 4q, 5q, 6q, 8q, and 13q and deletions at 1p, 9q, 16q, 17q, 19q, and 22q) in the follicular variant of PTC closely resembled that of FTA/FTC.]. 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:15188460 ;
    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:NP788473.RAI4bLbneUfku6REpbt0V5d6eib3xBjsBt3HRWdW0RZ_U130_publicationInfo {
   this: dcterms:created "2015-08-25T14:45:37+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" .
}