@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8
> .
@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:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_head
{
this:
np:hasAssertion
dgn-np:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_assertion
;
np:hasProvenance
dgn-np:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_provenance
;
np:hasPublicationInfo
dgn-np:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_assertion
a
np:Assertion
.
dgn-np:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_provenance
a
np:Provenance
.
dgn-np:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_assertion
{
miriam-gene:1041
a
ncit:C16612
.
lld:C0033860
a
ncit:C7057
.
dgn-gda:DGNf6cb43545321cafd0237e2b56bb8e23a
sio:SIO_000628
miriam-gene:1041
,
lld:C0033860
;
a
sio:SIO_001122
.
}
dgn-np:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_provenance
{
dgn-np:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_assertion
dct:description
"[In a case-control association study of psoriasis in the Sardinian population, we analyzed the allele distribution of eight intragenic SNPs (positions 619, 767, 1215, 1118, 1236, 1243, 1331, 1593) of the CDSN gene and the six haplotypes that are coded by these SNPs.]. 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:12472658
;
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:NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_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" .
}