@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE> .
@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:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_head {
  this: np:hasAssertion dgn-np:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_assertion;
    np:hasProvenance dgn-np:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_provenance;
    np:hasPublicationInfo dgn-np:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_assertion a np:Assertion .
  
  dgn-np:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_provenance a np:Provenance .
  
  dgn-np:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_assertion {
  miriam-gene:631 a ncit:C16612 .
  
  lld:C0086543 a ncit:C7057 .
  
  dgn-gda:DGN8798b1058840394446142bfa76f96344 sio:SIO_000628 miriam-gene:631, lld:C0086543;
    a sio:SIO_001121 .
}

dgn-np:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_provenance {
  dgn-np:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_assertion dcterms:description
      "[Mutations in both proteins cause lens cataract and careful consideration of the detail of these cataract phenotypes alerts us to several interesting features concerning the function of filensin (BFSP1) and CP49 (BFSP2) in the lens.]. 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:17490642;
    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:NP284645.RAlVpPc25CLc-cex5v7I1AYL8WmSA4NyMSFOTdCZ2iGeE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:40+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" .
}