@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48
> .
@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:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_head
{
this:
np:hasAssertion
dgn-np:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_assertion
;
np:hasProvenance
dgn-np:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_provenance
;
np:hasPublicationInfo
dgn-np:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_assertion
a
np:Assertion
.
dgn-np:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_provenance
a
np:Provenance
.
dgn-np:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0334590
a
ncit:C7057
.
dgn-gda:DGN707624d8b267a65f7d4787adf108d65e
sio:SIO_000628
miriam-gene:7157
,
lld:C0334590
;
a
sio:SIO_001121
.
}
dgn-np:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_provenance
{
dgn-np:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_assertion
dcterms:description
"[These findings demonstrate that oligodendroglial neoplasms usually have loss of 1p and 19q whereas astrocytomas of the progressive type frequently contain mutations of the TP53 gene, and that 9p loss and CDKN2A deletions are associated with progression from well-differentiated to anaplastic 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:10433931
;
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:NP442078.RAAKLMQBPYq6F4xCtgErtIv1z9cH4yrGdOop2azbWUd48130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:21+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" .
}