@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw> .
@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:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_head {
  this: np:hasAssertion dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_assertion ;
    np:hasProvenance dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_provenance ;
    np:hasPublicationInfo dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_assertion a np:Assertion .
  dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_provenance a np:Provenance .
  dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_assertion {
  miriam-gene:7291 a ncit:C16612 .
  lld:C0025362 a ncit:C7057 .
  dgn-gda:DGN82b1e60912d9767fe852d663961a01f7 sio:SIO_000628 miriam-gene:7291 , lld:C0025362 ;
    a sio:SIO_001121 .
}
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_provenance {
  dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_assertion dcterms:description "[These data definitively implicate perturbation of TGFbeta signaling in many common human phenotypes, including craniosynostosis, cleft palate, arterial aneurysms, congenital heart disease and mental retardation, and suggest that comprehensive mechanistic insight will require consideration of both primary and compensatory events.]. 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:15731757 ;
    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:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:57+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" .
}