@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_assertion
;
np:hasProvenance
dgn-np:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_provenance
;
np:hasPublicationInfo
dgn-np:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_assertion
a
np:Assertion
.
dgn-np:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_provenance
a
np:Provenance
.
dgn-np:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_assertion
{
miriam-gene:22861
a
ncit:C16612
.
lld:C1304470
a
ncit:C7057
.
dgn-gda:DGN915a1f49597e9618249c0f87a6c6d7a6
sio:SIO_000628
miriam-gene:22861
,
lld:C1304470
;
a
sio:SIO_001121
.
}
dgn-np:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_provenance
{
dgn-np:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_assertion
dcterms:description
"[We found that two SNPs in the NALP1 extended promoter region, rs1008588 and rs2670660 were significantly associated with generalized vitiligo in our cohort of Arab vitiligo patients, and several other SNPs in the NALP1 region were at the margin of significant association.]. 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:20574744
;
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:NP282257.RA0fzxHdjBXo7VALk_TYyatmzgqo1t0Wrsq_d63R9BzCE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}