@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms
> .
@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:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_head
{
this:
np:hasAssertion
dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_assertion
;
np:hasProvenance
dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_provenance
;
np:hasPublicationInfo
dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_assertion
a
np:Assertion
.
dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_provenance
a
np:Provenance
.
dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN1b7121cb0948d6d1f34c07e163bdd5a1
sio:SIO_000628
miriam-gene:673
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_provenance
{
dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_assertion
dcterms:description
"[While the frequency of KRAS mutations is comparable with other populations, absence of BRAF mutations is intriguing and would require further analysis of the molecular epidemiology of CRC in West Africa.]. 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:23962701
;
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:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}