@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A
> .
@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:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_head
{
this:
np:hasAssertion
dgn-np:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion
;
np:hasProvenance
dgn-np:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_provenance
;
np:hasPublicationInfo
dgn-np:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion
a
np:Assertion
.
dgn-np:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_provenance
a
np:Provenance
.
dgn-np:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion
{
miriam-gene:1017
a
ncit:C16612
.
lld:C0751396
a
ncit:C7057
.
dgn-gda:DGNc66f2fb0417269af7a97ff7ea4823a8f
sio:SIO_000628
miriam-gene:1017
,
lld:C0751396
;
a
sio:SIO_001121
.
}
dgn-np:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_provenance
{
dgn-np:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion
dcterms:description
"[Loss of 9p or homozygous deletion of the CDKN2 gene or both are associated with anaplastic oligodendrogliomas, whereas loss of 17p or TP53 gene mutations or both are frequent in astrocytomas, but rare in oligodendrogliomas.]. 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:11550302
;
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:NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}