@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc> .
@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:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_head {
   this: np:hasAssertion dgn-np:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_assertion ;
    np:hasProvenance dgn-np:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_provenance ;
    np:hasPublicationInfo dgn-np:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_assertion a np:Assertion .
  dgn-np:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_provenance a np:Provenance .
  dgn-np:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_assertion {
   miriam-gene:10457 a ncit:C16612 .
  lld:C1261473 a ncit:C7057 .
  dgn-gda:DGNcbe5d4ee68a1f0fc7bfb06002bfe7a8b sio:SIO_000628 miriam-gene:10457 , lld:C1261473 ;
    a sio:SIO_001121 .
}
dgn-np:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_provenance {
   dgn-np:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_assertion dcterms:description "[In situ hybridization for NMB gene expression on tissue microarrays (TMAs) containing a total of 1164 specimens representing 62 different sarcoma types and 15 different carcinoma types showed that NMB was highly expressed in 17 of 22 EMC cases and very rarely expressed in other tumours and thus could function as a novel diagnostic marker.]. 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:15920699 ;
    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:NP512207.RAVtwuuDwFZsqKFdQxHMxi0PZ6zALcM2YzvDDXaGL5Cyc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:05+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" .
}