@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI
> .
@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:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_head
{
this:
np:hasAssertion
dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_assertion
;
np:hasProvenance
dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_provenance
;
np:hasPublicationInfo
dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_assertion
a
np:Assertion
.
dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_provenance
a
np:Provenance
.
dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C1269683
a
ncit:C7057
.
dgn-gda:DGN571a6c53cd09feaba3fd494f5b005546
sio:SIO_000628
miriam-gene:1956
,
lld:C1269683
;
a
sio:SIO_001121
.
}
dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_provenance
{
dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_assertion
dcterms:description
"[EGFR mutations were associated with lower depression severity and lower rates of probable major depressive disorder in patients with metastatic NSCLC, based on mood screening performed before results of genotyping were known.]. 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:21807767
;
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:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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" .
}