@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA
> .
@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:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_head
{
this:
np:hasAssertion
dgn-np:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_assertion
;
np:hasProvenance
dgn-np:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_provenance
;
np:hasPublicationInfo
dgn-np:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_assertion
a
np:Assertion
.
dgn-np:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_provenance
a
np:Provenance
.
dgn-np:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_assertion
{
miriam-gene:1950
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGNa825478b3da21e5b80a601f5be03977e
sio:SIO_000628
miriam-gene:1950
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_provenance
{
dgn-np:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_assertion
dcterms:description
"[Epidermal growth factor (EGF) receptor (EGFR) mutations are the best illustration of the therapeutic relevance of identifying such molecular clusters of lung cancer based on driver genetic alterations that predict the efficacy of specific tyrosine kinase inhibitors, a strategy referred to as `personalized medicine.` Besides EGFR and ALK, other genes harboring driver molecular alterations have been identified as part of integrated genomic studies of lung cancers.]. 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:23307186
;
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:NP292608.RAdO5gxHSJvavG4C5XJaf8lpbI6V9qnOs8rMU1mkx4yLA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}