@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M> .
@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:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_head {
  this: np:hasAssertion dgn-np:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_assertion;
    np:hasProvenance dgn-np:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_provenance;
    np:hasPublicationInfo dgn-np:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_provenance a np:Provenance .
  
  dgn-np:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_assertion {
  miriam-gene:583 a ncit:C16612 .
  
  lld:C0152427 a ncit:C7057 .
  
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dgn-np:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_provenance {
  dgn-np:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_assertion dcterms:description
      "[A comparative study of the three Arab-Bedouin kindreds used to map the BBS2, BBS3, and BBS4 loci suggests that the variability in the number and severity of clinical manifestations, particularly the pattern of polydactyly, reflects chromosome-specific subtypes of BBS [Carmi et al., 1995a; Am J Med Genet 59:199-203].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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  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:NP687777.RAH8Xy8JAXRaMJrCS1IWjljk0Ficw1hRF1NkdVUWC7y7M130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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