@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA> .
@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:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_head {
  this: np:hasAssertion dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_assertion ;
    np:hasProvenance dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_provenance ;
    np:hasPublicationInfo dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_assertion a np:Assertion .
  dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_provenance a np:Provenance .
  dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_assertion {
  miriam-gene:3982 a ncit:C16612 .
  lld:C0086543 a ncit:C7057 .
  dgn-gda:DGNb80ddca772dc72f9e9130de794002cbe sio:SIO_000628 miriam-gene:3982 , lld:C0086543 ;
    a sio:SIO_001121 .
}
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_provenance {
  dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_assertion dcterms:description "[The fact that the MP19To3 did not traffic to the membrane, instead appearing to be trapped within a subcellular compartment within the cell sheds further light on the cause of the cataract and microphthalmia observed in the MP19To3 mutation, and further sheds information on the pathway of MP19 transport to the cell membrane.]. 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:12379840 ;
    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:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:15+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" .
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}