@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8
> .
@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/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_assertion
a
np:Assertion
.
dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_provenance
a
np:Provenance
.
dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_assertion
{
miriam-gene:8493
a
ncit:C16612
.
lld:C0242621
a
ncit:C7057
.
dgn-gda:DGNbaf81d61541f0dffcf018fdb69f89b8d
sio:SIO_000628
miriam-gene:8493
,
lld:C0242621
;
a
sio:SIO_001121
.
}
dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_provenance
{
dgn-np:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_assertion
dcterms:description
"[We examined primary medulloblastoma specimens and cell lines, and detected WIP1 copy gain and amplification prevalent among but not exclusively in the tumors with 17q gain and isochromosome 17q (i17q), which are among the most common cytogenetic lesions in medulloblastoma.]. 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:17932621
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP797047.RAGOWyAnxRreGrYaRPtPnkJ8zdYcTaw57Qgl7Wcx58qi8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:42+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
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;
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
}