@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI> .
@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:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_head {
  this: np:hasAssertion dgn-np:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_assertion ;
    np:hasProvenance dgn-np:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_provenance ;
    np:hasPublicationInfo dgn-np:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_assertion a np:Assertion .
  dgn-np:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_provenance a np:Provenance .
  dgn-np:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_assertion {
  miriam-gene:7905 a ncit:C16612 .
  lld:C0009402 a ncit:C7057 .
  dgn-gda:DGNdb5c93bb44232a923207924df83d3b06 sio:SIO_000628 miriam-gene:7905 , lld:C0009402 ;
    a sio:SIO_001121 .
}
dgn-np:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_provenance {
  dgn-np:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_assertion dcterms:description "[DNA from 61 primary Ewing tumors and 11 Ewing tumor cell lines was extracted and microsatellite analysis for the detection of instability or loss of heterozygosity was performed for the five markers of the Bethesda panel BAT25, BAT26, D5S346, D2S123, and D17S250, which represents the established marker panel for the analysis of hereditary non-polyposis colorectal carcinoma (HNPCC) patients.]. 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:17530287 ;
    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:NP909111.RAMwSSR6P8PKoxUeGW5s-EcU0D09sH0iRIAepSt5G7yNI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:18+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" .
}