@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek
> .
@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:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_head
{
this:
np:hasAssertion
dgn-np:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_assertion
;
np:hasProvenance
dgn-np:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_provenance
;
np:hasPublicationInfo
dgn-np:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_assertion
a
np:Assertion
.
dgn-np:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_provenance
a
np:Provenance
.
dgn-np:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_assertion
{
miriam-gene:2064
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGNf2e0fd3dbfe10741789d48e3eb27ce14
sio:SIO_000628
miriam-gene:2064
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_provenance
{
dgn-np:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_assertion
dcterms:description
"[Cancers with specific genetic abnormalities, for instance epidermal growth factor receptor (EGFR) mutant lung cancers and HER2 amplified breast cancers, are often sensitive to these new targeted therapies that can specifically inhibit the function of EGFR or HER2.]. 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:22959036
;
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:NP394673.RABDUT5tk7MgzXbiuob7mHaIFwAukjBo9sU5sTSDm5xek130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}