@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_head
{
this:
np:hasAssertion
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_assertion
;
np:hasProvenance
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_assertion
a
np:Assertion
.
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_provenance
a
np:Provenance
.
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGNeaaa4d5af346127cf8e8e8865658566a
sio:SIO_000628
miriam-gene:1956
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_provenance
{
dgn-np:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_assertion
dcterms:description
"[Interestingly, the extent of these SHP2 signaling regulatory functions is diminished in glioblastoma cells that express sufficiently high levels of the EGFR variant III (EGFRvIII) mutant, which is commonly expressed in GBM.]. 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:24951116
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1194322.RAGmN1mSENn-B9bUNcAjyLt-o61Q9ABJDNo8gjhfStiKQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:47+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}