@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg
> .
@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:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_head
{
this:
np:hasAssertion
dgn-np:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_assertion
;
np:hasProvenance
dgn-np:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_provenance
;
np:hasPublicationInfo
dgn-np:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_assertion
a
np:Assertion
.
dgn-np:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_provenance
a
np:Provenance
.
dgn-np:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0854983
a
ncit:C7057
.
dgn-gda:DGN10a8cba9eac5aa90737b8b404167b8d0
sio:SIO_000628
miriam-gene:1956
,
lld:C0854983
;
a
sio:SIO_001121
.
}
dgn-np:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_provenance
{
dgn-np:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_assertion
dcterms:description
"[Although specific clinical circumstances should guide therapy, our cost-effectiveness analysis supports the strategy of testing for EGFR mutations in patients with stage IV or recurrent adenocarcinoma of the lung, rebiopsying patients if insufficient tissue is available for testing, and treating patients with EGFR mutations with erlotinib as first-line therapy.]. 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:23277762
;
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:NP823488.RAmjvw9ZIve47yMnAQmY_HU2fWGpNkr-yLH6Z3teXNUTg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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" .
}