@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY
> .
@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:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_head
{
this:
np:hasAssertion
dgn-np:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_assertion
;
np:hasProvenance
dgn-np:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_provenance
;
np:hasPublicationInfo
dgn-np:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_assertion
a
np:Assertion
.
dgn-np:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_provenance
a
np:Provenance
.
dgn-np:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_assertion
{
miriam-gene:3127
a
ncit:C16612
.
lld:C0018213
a
ncit:C7057
.
dgn-gda:DGN1d7b012c9538926af18838a60907996f
sio:SIO_000628
miriam-gene:3127
,
lld:C0018213
;
a
sio:SIO_001121
.
}
dgn-np:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_provenance
{
dgn-np:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_assertion
dcterms:description
"[The human leukocyte antigen class II genes DRB1, DQB1, and DQA1 are associated with Graves disease (GD), but, because of strong linkage disequilibrium within this region, the primary etiological variant(s) remains unknown.]. 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:15558498
;
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:NP797915.RATOvdmLFgGa6JebjayWMc3YLtJVqfCcPm4l3RGkIMVwY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}