@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc
> .
@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:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_head
{
this:
np:hasAssertion
dgn-np:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_assertion
;
np:hasProvenance
dgn-np:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_provenance
;
np:hasPublicationInfo
dgn-np:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_assertion
a
np:Assertion
.
dgn-np:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_provenance
a
np:Provenance
.
dgn-np:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C1520166
a
ncit:C7057
.
dgn-gda:DGN8ec8975b589cb0d4ef00893c27b98fec
sio:SIO_000628
miriam-gene:5290
,
lld:C1520166
;
a
sio:SIO_001121
.
}
dgn-np:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_provenance
{
dgn-np:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_assertion
dcterms:description
"[Specifically, introduction of a subset of the mutations identified in human GBM, in the nSH2 and iSH2 domains, increases signaling through the PI3K pathway and promotes tumorigenesis of primary normal human astrocytes in an orthotopic xenograft model.]. 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:23166678
;
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:NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:08+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" .
}