@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U
> .
@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:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_head
{
this:
np:hasAssertion
dgn-np:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_assertion
;
np:hasProvenance
dgn-np:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_provenance
;
np:hasPublicationInfo
dgn-np:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_assertion
a
np:Assertion
.
dgn-np:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_provenance
a
np:Provenance
.
dgn-np:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0334583
a
ncit:C7057
.
dgn-gda:DGN8007da6530193eb60769c9ef54b804e5
sio:SIO_000628
miriam-gene:7157
,
lld:C0334583
;
a
sio:SIO_001121
.
}
dgn-np:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_provenance
{
dgn-np:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_assertion
dcterms:description
"[Using sequencing and/or immunohistochemical analyses, we investigated ATRX alterations (mutation/loss of expression) and their association with TP53 and IDH1 or IDH2 mutations in 140 adult WHO grade II, III and IV gliomas, 17 pediatric WHO grade II and III astrocytomas and 34 pilocytic astrocytomas.]. 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:22886134
;
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:NP644733.RAksTfUE5Q7xhyfvc9uXZPbelj2N3HKqNzaRp00JhbW2U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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" .
}