@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4
> .
@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:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_head
{
this:
np:hasAssertion
dgn-np:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_assertion
;
np:hasProvenance
dgn-np:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_provenance
;
np:hasPublicationInfo
dgn-np:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_assertion
a
np:Assertion
.
dgn-np:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_provenance
a
np:Provenance
.
dgn-np:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0040128
a
ncit:C7057
.
dgn-gda:DGNa1a72676f41d59ae5f0e5344cbef93d2
sio:SIO_000628
miriam-gene:3133
,
lld:C0040128
;
a
sio:SIO_001121
.
}
dgn-np:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_provenance
{
dgn-np:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_assertion
dcterms:description
"[MS patients had slightly higher rates of thyroid disease and pernicious anaemia than did controls, which is consistent with MHC associations for these diseases, but this effect disappeared when results were adjusted for sex.]. 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:17560172
;
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:NP563278.RAPZj-T2DIED9m_FNrBmlSYWaTVtmkJ1zLZGT4ZnrvHw4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}