@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM> .
@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:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_head {
   this: np:hasAssertion dgn-np:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_assertion ;
    np:hasProvenance dgn-np:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_provenance ;
    np:hasPublicationInfo dgn-np:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_assertion a np:Assertion .
  dgn-np:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_provenance a np:Provenance .
  dgn-np:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_assertion {
   miriam-gene:4683 a ncit:C16612 .
  lld:C0085078 a ncit:C7057 .
  dgn-gda:DGN70af46bb377c5913a0e21c0985588e51 sio:SIO_000628 miriam-gene:4683 , lld:C0085078 ;
    a sio:SIO_001121 .
}
dgn-np:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_provenance {
   dgn-np:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_assertion dcterms:description "[Taking into account that several LSDs were identified in a higher frequency in selected areas and/or populations, the population medical genetics approach could help to introduce the NBS for LSDs in the region, with identification of areas with higher risk for selected diseases and design of customized screening program to address specific needs.]. 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:22231381 ;
    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:NP742583.RAMZJN91H8qjHkP6cBtKoi3QbzLKoc5Y58bHHtHA5CuzM130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:30+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" .
}