@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k
> .
@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:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_head
{
this:
np:hasAssertion
dgn-np:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_assertion
;
np:hasProvenance
dgn-np:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_provenance
;
np:hasPublicationInfo
dgn-np:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_assertion
a
np:Assertion
.
dgn-np:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_provenance
a
np:Provenance
.
dgn-np:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN3456816aa453494c80334fa46ca131a4
sio:SIO_000628
miriam-gene:3845
,
lld:C0009402
;
a
sio:SIO_001122
.
}
dgn-np:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_provenance
{
dgn-np:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_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:NP794331.RAMwImfIFkm-Wf1PjTuO1RNUgY6D36A_McMKVgQUo6c4k130_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" .
}