@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0
> .
@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:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_head
{
this:
np:hasAssertion
dgn-np:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_assertion
;
np:hasProvenance
dgn-np:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_provenance
;
np:hasPublicationInfo
dgn-np:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_assertion
a
np:Assertion
.
dgn-np:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_provenance
a
np:Provenance
.
dgn-np:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0206726
a
ncit:C7057
.
dgn-gda:DGNdce0d2a0a5dfb5404464622274a5bd40
sio:SIO_000628
miriam-gene:7157
,
lld:C0206726
;
a
sio:SIO_001121
.
}
dgn-np:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_provenance
{
dgn-np:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_assertion
dcterms:description
"[Unusual findings include: TP53 mutation in a juvenile pilocytic astrocytoma; TP53 and PTEN mutations in a de novo glioblastoma, a gliosarcoma with identical mutations in gliomatous and sarcomatous components, and an infratentorial anaplastic astrocytoma with an earlier supratentorial grade II astrocytoma bearing the same TP53 mutation but not the PTEN mutation or loss of heterozygosity (LOH) of 10q23.]. 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:11355303
;
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:NP770139.RA0c_WjdJwAP234IJAHve5dOZZDeNSH1N8I5YI_gv93x0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}