@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w
> .
@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:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_head
{
this:
np:hasAssertion
dgn-np:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_assertion
;
np:hasProvenance
dgn-np:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_provenance
;
np:hasPublicationInfo
dgn-np:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_assertion
a
np:Assertion
.
dgn-np:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_provenance
a
np:Provenance
.
dgn-np:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0278517
a
ncit:C7057
.
dgn-gda:DGN224f0b0add99bb875b43141456b202e4
sio:SIO_000628
miriam-gene:1956
,
lld:C0278517
;
a
sio:SIO_001122
.
}
dgn-np:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_provenance
{
dgn-np:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_assertion
dcterms:description
"[Elderly patients aged 75 or older with advanced or recurrent NSCLC and EGFR mutations (exon 19 deletion or L858R mutation in exon 21) were enrolled in this prospective phase II trial.]. 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:26003540
;
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:NP1285262.RAG-piE90HRQLntbugVeRbvu2KphMmiaqoqpXttd9RF8w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:28+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" .
}