@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88
> .
@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:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_head
{
this:
np:hasAssertion
dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_assertion
;
np:hasProvenance
dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_provenance
;
np:hasPublicationInfo
dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_assertion
a
np:Assertion
.
dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_provenance
a
np:Provenance
.
dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN42839cee207f5bce11741dbe0a7cbe76
sio:SIO_000628
miriam-gene:3845
,
lld:C1527249
;
a
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.
}
dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_provenance
{
dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_assertion
dcterms:description
"[The study suggests that activating KRAS mutants is a particularly important independent predictive marker in mCRC patients treated with cetuximab plus chemotherapy, of which combing activating KRAS mutants and EGFR could help to identify the subgroup of patients who are most likely to respond to cetuximab plus chemotherapy.]. 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:20010090
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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
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pav:authoredBy
<
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> , <
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> , <
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
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}