@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8
> .
@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:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_head
{
this:
np:hasAssertion
dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_assertion
;
np:hasProvenance
dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_provenance
;
np:hasPublicationInfo
dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_assertion
a
np:Assertion
.
dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_provenance
a
np:Provenance
.
dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGNbfc8587cce4fb957730ba0a8bd8afd62
sio:SIO_000628
miriam-gene:1956
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_provenance
{
dgn-np:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_assertion
dcterms:description
"[Thus, understanding how activating mutations in the TKD domain of EGFR contribute to radiosensitivity should provide new insight into effective treatment of NSCLC with radiotherapy and perhaps avoid emergence of single agent drug resistance.]. 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:17018617
;
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:NP572782.RAOfcFN5TAedK84-i-HtuLdLpl9C0vWq4ZRxMtpz3e-p8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:04+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" .
}