@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8> .
@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:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_head {
  this: np:hasAssertion dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_assertion ;
    np:hasProvenance dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_provenance ;
    np:hasPublicationInfo dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_assertion a np:Assertion .
  dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_provenance a np:Provenance .
  dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_assertion {
  miriam-gene:3356 a ncit:C16612 .
  lld:C0003125 a ncit:C7057 .
  dgn-gda:DGN8a7324ebf90b6dd2e4d47e140e9cad04 sio:SIO_000628 miriam-gene:3356 , lld:C0003125 ;
    a sio:SIO_001121 .
}
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_provenance {
  dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_assertion dcterms:description "[Although, at present, no convincing evidence for associations of candidate genes with EDs has been provided, the 5-HT(2A) receptor gene and the BDNF gene seem to be promising candidates for genetic influences on AN, since polymorphic variants of these genes have been found quite consistently, although not specifically, linked to AN restricting subtype in large sample studies.]. 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:18855537 ;
    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:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:16+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" .
}