@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_head {
  this: np:hasAssertion dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_assertion ;
    np:hasProvenance dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_provenance ;
    np:hasPublicationInfo dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_assertion a np:Assertion .
  dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_provenance a np:Provenance .
  dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_assertion {
  miriam-gene:84894 a ncit:C16612 .
  lld:C0270736 a ncit:C7057 .
  dgn-gda:DGN3ddd8352e1faad637f64db07004b9517 sio:SIO_000628 miriam-gene:84894 , lld:C0270736 ;
    a sio:SIO_001122 .
}
dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_provenance {
  dgn-np:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_assertion dcterms:description "[Recently, the first genome-wide association study in ET followed by replication studies conducted in diverse populations identified a significant association between the leucine-rich repeat and Ig domain containing 1 gene (LINGO1) SNP rs9652490 and risk for ET Although further novel variants were indentified in LINGO1 and its paralog LINGO2 that may be associated with risk for ET, the pathogenic mechanisms involved remain elusive.]. 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:22166413 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP946295.RAYE8L3fIeC65X5HUxOqnbXd_pnlMcip6fBst9C2GWVEs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:54+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}