@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY
> .
@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:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_head
{
this:
np:hasAssertion
dgn-np:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_assertion
;
np:hasProvenance
dgn-np:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_provenance
;
np:hasPublicationInfo
dgn-np:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_assertion
a
np:Assertion
.
dgn-np:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_provenance
a
np:Provenance
.
dgn-np:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_assertion
{
miriam-gene:1111
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN2fad7ff85bf5f93cc4baa2b68a802b6c
sio:SIO_000628
miriam-gene:1111
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_provenance
{
dgn-np:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_assertion
dcterms:description
"[The cell cycle checkpoint kinase 2 (CHEK2) gene I157T variant may be associated with an increased risk of colorectal cancer, but it is unclear whether the evidence is sufficient to recommend testing for the mutation in clinical practice.]. 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:22901170
;
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:NP723004.RAF1RLrjNQWu5EU7xJ0F_OUo9F9Raizhv_1LJmVcTnzbY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}