@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU
> .
@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:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_head
{
this:
np:hasAssertion
dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_assertion
;
np:hasProvenance
dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_provenance
;
np:hasPublicationInfo
dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_assertion
a
np:Assertion
.
dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_provenance
a
np:Provenance
.
dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_assertion
{
miriam-gene:10392
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN9c501bdf04e39821a4550a5031c0c7fb
sio:SIO_000628
miriam-gene:10392
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_provenance
{
dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_assertion
dct:description
"[Since the CARD15 gene product and other CARD proteins function in innate immunity, we investigated the impact of germline variation at the CARD4, CARD8 and CARD15 loci on the risk for sporadic CRC, using a large patient sample from Northern Germany.]. 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:19843337
;
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:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:38+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" .
}