@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY
> .
@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:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_head
{
this:
np:hasAssertion
dgn-np:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_assertion
;
np:hasProvenance
dgn-np:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_provenance
;
np:hasPublicationInfo
dgn-np:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_assertion
a
np:Assertion
.
dgn-np:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_provenance
a
np:Provenance
.
dgn-np:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_assertion
{
miriam-gene:56246
a
ncit:C16612
.
lld:C0701807
a
ncit:C7057
.
dgn-gda:DGN4d14b872bb45f2156908f15c67f7f84f
sio:SIO_000628
miriam-gene:56246
,
lld:C0701807
;
a
sio:SIO_001121
.
}
dgn-np:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_provenance
{
dgn-np:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_assertion
dcterms:description
"[In the absence of evidence of linkage disequilibrium between A2 and B27 in the general population, the data suggest that the presence of A2 in B27 positive AS patients enhances the risk of AAU above that associated with B27 alone, and that other MHC-linked genetic factors, in addition to B27, are associated with susceptibility to AAU in AS patients.]. 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:7194916
;
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:NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}