@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI> .
@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:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_head {
  this: np:hasAssertion dgn-np:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_assertion;
    np:hasProvenance dgn-np:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_provenance;
    np:hasPublicationInfo dgn-np:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_assertion a np:Assertion .
  
  dgn-np:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_provenance a np:Provenance .
  
  dgn-np:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_assertion {
  miriam-gene:373159 a ncit:C16612 .
  
  lld:C0035334 a ncit:C7057 .
  
  dgn-gda:DGN1abdc61ac4b362e76021fbbd5636bd25 sio:SIO_000628 miriam-gene:373159, lld:C0035334;
    a sio:SIO_001121 .
}

dgn-np:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_provenance {
  dgn-np:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_assertion dcterms:description
      "[About 10% recombination has been found between the retinitis pigmentosa locus (RP2) and the marker locus DXS7, assigned to band Xp11.3, which was reported earlier to be closely linked to RP2 in several independent families.]. 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:3397063;
    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:NP649456.RANvdbPidYx_NStGCBqEmLnTCaccSVhZWzsWFeuRxTzZI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:31+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" .
}