@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8
> .
@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:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_head
{
this:
np:hasAssertion
dgn-np:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_assertion
;
np:hasProvenance
dgn-np:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_provenance
;
np:hasPublicationInfo
dgn-np:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_assertion
a
np:Assertion
.
dgn-np:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_provenance
a
np:Provenance
.
dgn-np:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_assertion
{
miriam-gene:170679
a
ncit:C16612
.
lld:C0033860
a
ncit:C7057
.
dgn-gda:DGNef08d8ad10248959e67ac307567a1294
sio:SIO_000628
miriam-gene:170679
,
lld:C0033860
;
a
sio:SIO_001121
.
}
dgn-np:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_provenance
{
dgn-np:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_assertion
dcterms:description
"[Because the +39604 SEEK1 polymorphism in chromosome 6p has recently been associated with psoriasis, the prevalence of this polymorphism, as well as two additional single nucleotide polymorphisms in the SEEK1 gene, in patients with CD from the Newfoundland population were determined.]. 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:15301859
;
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:NP222813.RAqHXtnBRFS6l13GN-psKJn9rshyRjk9q6teHqweYRur8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}