@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo
> .
@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:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_head
{
this:
np:hasAssertion
dgn-np:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_assertion
;
np:hasProvenance
dgn-np:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_provenance
;
np:hasPublicationInfo
dgn-np:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_assertion
a
np:Assertion
.
dgn-np:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_provenance
a
np:Provenance
.
dgn-np:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0036421
a
ncit:C7057
.
dgn-gda:DGNfe03f8c3c3546f8a1a73aad386f108ca
sio:SIO_000628
miriam-gene:6520
,
lld:C0036421
;
a
sio:SIO_001121
.
}
dgn-np:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_provenance
{
dgn-np:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_assertion
dcterms:description
"[To investigate the relationship of the polymorphic enhancer HS1,2 central to the 3' enhancer complex regulatory region (IgH3'EC) of the immunoglobulin heavy chain genes with systemic sclerosis (SSc) disease and compare it with HLA-DR and DQ associations.]. 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:17392350
;
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:NP191913.RA4K8ji6u9YeoE6WWcI8KFZY-P832cvE1Lk_pe1rgAqMo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}