@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_head
{
this:
np:hasAssertion
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_assertion
;
np:hasProvenance
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_provenance
;
np:hasPublicationInfo
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_assertion
a
np:Assertion
.
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_provenance
a
np:Provenance
.
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNc609be30adc9928bdb9f5df70cfa77cf
sio:SIO_000628
miriam-gene:3845
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_provenance
{
dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_assertion
dcterms:description
"[Specific KRAS mutation is an informative prognostic factor in both sporadic and hereditary CRC and applied in an algorithm with BRAF(V600E) and MSI may identify sporadic CRC patients with poor clinical outcome.]. 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:20162668
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:45+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}