@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc
> .
@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:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_head
{
this:
np:hasAssertion
dgn-np:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_assertion
;
np:hasProvenance
dgn-np:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_provenance
;
np:hasPublicationInfo
dgn-np:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_assertion
a
np:Assertion
.
dgn-np:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_provenance
a
np:Provenance
.
dgn-np:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_assertion
{
miriam-gene:4261
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN413b431e4b6d85e0135fd4fada20a6df
sio:SIO_000628
miriam-gene:4261
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_provenance
{
dgn-np:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_assertion
dcterms:description
"[Single-nucleotide polymorphisms (SNPs) in the major histocompatibility complex class II transactivator (MHC2TA) gene encoding the class II transactivator have been associated with multiple sclerosis, rheumatoid arthritis, and myocardial infarction in the Swedish population.]. 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:17711409
;
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:NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}