@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc
> .
@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:NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc130_assertion
a
np:Assertion
.
dgn-np:NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc130_provenance
a
np:Provenance
.
dgn-np:NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0220668
a
ncit:C7057
.
dgn-gda:DGN4e372a5f089705d7c6f6311fa1647e7b
sio:SIO_000628
miriam-gene:3845
,
lld:C0220668
;
a
sio:SIO_001121
.
}
dgn-np:NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc130_provenance
{
dgn-np:NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc130_assertion
dcterms:description
"[Our findings indicate that somatic mutations in KRAS and PIK3CA but not BRAF oncogenes are closely associated with the development of CCA in Chinese population and provide new potential targets for future therapeutic treatments of the disease.]. 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:21051183
;
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:NP696091.RAkj230_QI3ChXZde__iXanfQONgJspQRHNFUPLm-GERc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}