@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU
> .
@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:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_head
{
this:
np:hasAssertion
dgn-np:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_assertion
;
np:hasProvenance
dgn-np:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_provenance
;
np:hasPublicationInfo
dgn-np:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_assertion
a
np:Assertion
.
dgn-np:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_provenance
a
np:Provenance
.
dgn-np:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_assertion
{
miriam-gene:4261
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGNa72c025ff31d86e53343e55383da1410
sio:SIO_000628
miriam-gene:4261
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_provenance
{
dgn-np:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_assertion
dcterms:description
"[We analysed whether the single nucleotide polymorphism (SNP) rs3087456 in the promoter of the MHC class II transactivator (MHC2TA) gene is associated with manifestation of rheumatoid arthritis, multiple sclerosis, narcolepsy and Wegener granulomatosis.]. 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:16426246
;
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:NP269084.RAQaRIlNywh8AUSZmYOllo2An8zTkEo7VusaEwgWf_5aU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}