@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4
> .
@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:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_head
{
this:
np:hasAssertion
dgn-np:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_assertion
;
np:hasProvenance
dgn-np:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_provenance
;
np:hasPublicationInfo
dgn-np:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_assertion
a
np:Assertion
.
dgn-np:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_provenance
a
np:Provenance
.
dgn-np:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_assertion
{
miriam-gene:7294
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGN417b565f4f3786ecaba94b755baaa397
sio:SIO_000628
miriam-gene:7294
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_provenance
{
dgn-np:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_assertion
dcterms:description
"[The presence of epidermal growth factor receptor (EGFR) tyrosine kinase (TK) mutations significantly correlates with tumor sensitivity to TK inhibitors, particularly in lung adenocarcinomas, the predominant histological subtype in Japan and the United States.]. 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:18571764
;
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:NP399412.RAemj4m-LcrpZsk1pVAKocYwq_FsimgXJJaA_CBfFinK4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}