@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM
> .
@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:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_head
{
this:
np:hasAssertion
dgn-np:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_assertion
;
np:hasProvenance
dgn-np:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_provenance
;
np:hasPublicationInfo
dgn-np:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_assertion
a
np:Assertion
.
dgn-np:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_provenance
a
np:Provenance
.
dgn-np:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_assertion
{
miriam-gene:10763
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN817e2f803677c847f8df2221103d66ff
sio:SIO_000628
miriam-gene:10763
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_provenance
{
dgn-np:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_assertion
dcterms:description
"[We demonstrate that expression of a constitutively active, mutant form of EGFR in cells in the glial lineage can induce lesions with many similarities to human gliomas, including increased cell density, vascular proliferation, and immunohistochemical staining for glial fibrillary acidic protein (GFAP) and nestin.]. 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:10669005
;
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:NP463430.RAi7FByXNRM7BeWdYmyDE6wUI36ad2Qi8dLeD1mZ968lM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:36+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" .
}