@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw
> .
@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 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:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_head
{
this:
np:hasAssertion
dgn-np:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_assertion
;
np:hasProvenance
dgn-np:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_provenance
;
np:hasPublicationInfo
dgn-np:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_assertion
a
np:Assertion
.
dgn-np:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_provenance
a
np:Provenance
.
dgn-np:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNbf7f3e0faa33ec5941ede3eed1e9920e
sio:SIO_000628
miriam-gene:673
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_provenance
{
dgn-np:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_assertion
dct:description
"[Using a collection of 225 colorectal cancers from 2 prospective cohort studies, we examined the relationship between NRAS mutations, clinical outcome, and other molecular features, including mutation of KRAS, BRAF, and PIK3CA, microsatellite instability, and the CpG island methylator phenotype.]. 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:20736745
;
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:NP59707.RA9SagiQZto_q6qD3SeRglztfv-Es0OascZYzwbg0R9dw130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}