@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q
> .
@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:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_head
{
this:
np:hasAssertion
dgn-np:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_assertion
;
np:hasProvenance
dgn-np:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_assertion
a
np:Assertion
.
dgn-np:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_provenance
a
np:Provenance
.
dgn-np:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN9712125f5380d39dbbfae7bfe66db0bb
sio:SIO_000628
miriam-gene:1956
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_provenance
{
dgn-np:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_assertion
dcterms:description
"[This study has an overall implication for establishing relevance for routine EGFR mutation diagnostics for NSCLC patients in clinics and emphasizes effectiveness for adoption of EGFR inhibitors as the first line treatment among Indian population.]. 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:24124538
;
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:NP1119099.RALhkjNPWv8ZaGFcBq2qhe2mYfyLIrczcWDFFhmQBBF6Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:13+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" .
}