@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI> .
@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:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_head {
  this: np:hasAssertion dgn-np:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_assertion;
    np:hasProvenance dgn-np:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_provenance;
    np:hasPublicationInfo dgn-np:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_assertion a np:Assertion .
  
  dgn-np:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_provenance a np:Provenance .
  
  dgn-np:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_assertion {
  miriam-gene:3351 a ncit:C16612 .
  
  lld:C0005941 a ncit:C7057 .
  
  dgn-gda:DGN341a79ff480e91a9b71a0c9d6b543c14 sio:SIO_000628 miriam-gene:3351, lld:C0005941;
    a sio:SIO_001121 .
}

dgn-np:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_provenance {
  dgn-np:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_assertion dcterms:description
      "[We could not find disease-causing coding variants in neither of the tested genes and therefore, we cannot provide support for an important function of TPH1 and HTR1B in the pathogenesis of sclerosing bone dysplasias in our tested patient cohort.]. 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:23563356;
    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:NP320772.RA2t1em2j92kOADY-yBb10cK7um6n7IRt4vyILTTg9PzI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:06+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" .
}