@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_head {
  this: np:hasAssertion dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_assertion ;
    np:hasProvenance dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_provenance ;
    np:hasPublicationInfo dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_assertion a np:Assertion .
  dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_provenance a np:Provenance .
  dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_assertion {
  miriam-gene:5727 a ncit:C16612 .
  lld:C0025149 a ncit:C7057 .
  dgn-gda:DGN8ca49f3e3c89f04bdf7356b322cb7aab sio:SIO_000628 miriam-gene:5727 , lld:C0025149 ;
    a sio:SIO_001121 .
}
dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_provenance {
  dgn-np:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_assertion dcterms:description "[One of the two mutations detected in this study had been missed by SSCP, suggesting that the true rate of PTCH mutations in sporadic medulloblastomas may be underestimated by SSCP screening.]. 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:10874314 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP287842.RAVplLgtp6R5OjJb1y67sLdKOfNWU3IkE2_EKbraSeTtc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:56+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}