@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY
> .
@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:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_head
{
this:
np:hasAssertion
dgn-np:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_assertion
;
np:hasProvenance
dgn-np:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_provenance
;
np:hasPublicationInfo
dgn-np:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_assertion
a
np:Assertion
.
dgn-np:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_provenance
a
np:Provenance
.
dgn-np:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0004114
a
ncit:C7057
.
dgn-gda:DGNfb9f39f0c75298282b6056ee2b4ae640
sio:SIO_000628
miriam-gene:1956
,
lld:C0004114
;
a
sio:SIO_001121
.
}
dgn-np:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_provenance
{
dgn-np:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_assertion
dcterms:description
"[EGFR overexpression is the most frequent and important molecular event in the development of astrocytic gliomas, and the P13K signaling pathway is one of the most important downstream pathways of EGFR.]. 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:16700623
;
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:NP273619.RAjIbGRrjmDrnSPf6tE4z5_Phx472U_8ThREwmISaO5nY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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" .
}