@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c
> .
@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 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:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_head
{
this:
np:hasAssertion
dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_assertion
;
np:hasProvenance
dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_assertion
a
np:Assertion
.
dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_provenance
a
np:Provenance
.
dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN4aa8cf469b6aa601889e26a3352bbece
sio:SIO_000628
miriam-gene:64127
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_provenance
{
dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_assertion
dct:description
"[The CARD15 R702W variant might be a predisposing factor to sporadic CRC in Portugal, particularly in patients under 60-years old and in female patients. This susceptibility appears to be linked with germline CARD15 mutations. Nevertheless, we have found no evidence that CARD15 mutations predict the pathologic characteristics of CRC.]. 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:20676658
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}