@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc> .
@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:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_head {
  this: np:hasAssertion dgn-np:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_assertion ;
    np:hasProvenance dgn-np:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_provenance ;
    np:hasPublicationInfo dgn-np:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_assertion a np:Assertion .
  dgn-np:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_provenance a np:Provenance .
  dgn-np:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_assertion {
  miriam-gene:7253 a ncit:C16612 .
  lld:C0700502 a ncit:C7057 .
  dgn-gda:DGNd0845ef19d1ac6e269f3a9b1989d94f2 sio:SIO_000628 miriam-gene:7253 , lld:C0700502 ;
    a sio:SIO_001121 .
}
dgn-np:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_provenance {
  dgn-np:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_assertion dcterms:description "[The epitope of blocking TSHRAbs with the ability to inhibit TSH binding (TBII activity), TSH activity, and stimulating TSHRAb activity, and that are causally implicated in the primary hypothyroidism of patients with idiopathic myxedema or some patients with Hashimoto's disease have, in contrast, been largely identified largely on the C-terminal portion of the TSHR extracellular domain, residues 270-395.]. 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:14669940 ;
    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:NP227891.RAmXzm7_h_bRBNWXkx2A8fJ7r9STs3AtmMdutmV1DgkXc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:06+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" .
}