@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y> .
@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:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_head {
  this: np:hasAssertion dgn-np:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_assertion;
    np:hasProvenance dgn-np:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_provenance;
    np:hasPublicationInfo dgn-np:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_assertion a np:Assertion .
  
  dgn-np:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_provenance a np:Provenance .
  
  dgn-np:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_assertion {
  miriam-gene:7276 a ncit:C16612 .
  
  lld:C0206246 a ncit:C7057 .
  
  dgn-gda:DGN306e511e1bef40da66172e8e9467c8e1 sio:SIO_000628 miriam-gene:7276, lld:C0206246;
    a sio:SIO_001121 .
}

dgn-np:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_provenance {
  dgn-np:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_assertion dcterms:description
      "[Vitreous amyloidosis is a rare condition that occurs in some forms of Transthyretin hereditary Amyloidosis, mainly in Familial Amyloidotic Polyneuropathy type I. Vitreous opacities may be the earliest occurring or, in some cases, only symptom of this disorder.]. 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:8063479;
    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:NP270871.RAd2cYicsPhpgXQ_IonVWDJJULypqfBz_LkmbkSkQ4p6Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:31+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" .
}