@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E> .
@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:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_head {
  this: np:hasAssertion dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_assertion ;
    np:hasProvenance dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_provenance ;
    np:hasPublicationInfo dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_assertion a np:Assertion .
  dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_provenance a np:Provenance .
  dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  lld:C0085136 a ncit:C7057 .
  dgn-gda:DGNb0e4424fc70f2f5a10a0cd24b0600885 sio:SIO_000628 miriam-gene:4771 , lld:C0085136 ;
    a sio:SIO_001121 .
}
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_provenance {
  dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_assertion dcterms:description "[Mutations of the neurofibromatosis 2 (NF2) tumor suppressor gene have frequently been detected not only in schwannomas and other central nervous system tumors of NF2 patients but also in their sporadic counterparts and malignant tumors unrelated to the NF2 syndrome such as malignant mesothelioma, indicating a broader role for the NF2 gene in human tumorigenesis.]. 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:17210637 ;
    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:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:48+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" .
}