@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs
> .
@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:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_head
{
this:
np:hasAssertion
dgn-np:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_assertion
;
np:hasProvenance
dgn-np:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_provenance
;
np:hasPublicationInfo
dgn-np:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_assertion
a
np:Assertion
.
dgn-np:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_provenance
a
np:Provenance
.
dgn-np:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN03f08ff7150a3fae2d61536928e6570d
sio:SIO_000628
miriam-gene:673
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_provenance
{
dgn-np:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_assertion
dcterms:description
"[Our data document (a) the absence of BRAF mutations in cervical and endometrial cancer, despite the mutation status of KRAS, (b) suggest that KRAS mutations reflect an early event in endometrial carcinogenesis and (c) imply that BRAF activation is involving alternative pathways in these two types of cancer.]. 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:16256179
;
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:NP587468.RAmMeRqIMfT5iKwOAr3W7Rm4H08HMyZoaZLwvsvgFamvs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}