@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8> .
@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:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_head {
  this: np:hasAssertion dgn-np:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_assertion ;
    np:hasProvenance dgn-np:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_provenance ;
    np:hasPublicationInfo dgn-np:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_assertion a np:Assertion .
  dgn-np:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_provenance a np:Provenance .
  dgn-np:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_assertion {
  miriam-gene:65250 a ncit:C16612 .
  lld:C0431399 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_provenance {
  dgn-np:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_assertion dcterms:description "[Our study, the largest comprehensive molecular series on JS, provides independent confirmation of the recently reported TCTN1, TMEM237, and C5ORF42 as bona fide JS disease genes, and expands the allelic heterogeneity of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP372314.RAJpkMMxcI0O8NPQyuJtEjpD9dJ-3qadrukYDL_UXFGq8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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 ;
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}