@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE> .
@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:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_head {
  this: np:hasAssertion dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_assertion ;
    np:hasProvenance dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_provenance ;
    np:hasPublicationInfo dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_assertion a np:Assertion .
  dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_provenance a np:Provenance .
  dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_assertion {
  miriam-gene:4901 a ncit:C16612 .
  lld:C0339526 a ncit:C7057 .
  dgn-gda:DGN84d6cbf4a95d7ec082f81a050df1447a sio:SIO_000628 miriam-gene:4901 , lld:C0339526 ;
    a sio:SIO_001121 .
}
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_provenance {
  dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_assertion dcterms:description "[Since a locus for autosomal recessive retinitis pigmentosa (arRP) has been linked to markers at 14q11 and since mutations in rhodopsin can lead to RP, we sequenced genomic PCR products of the NRL gene and of the rhodopsin-Nrl response element from a panel of patients representing independent families with inherited retinal degeneration.]. 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:9344665 ;
    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:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:20+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" .
}