@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI
> .
@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:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_head
{
this:
np:hasAssertion
dgn-np:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_assertion
;
np:hasProvenance
dgn-np:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_provenance
;
np:hasPublicationInfo
dgn-np:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_assertion
a
np:Assertion
.
dgn-np:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_provenance
a
np:Provenance
.
dgn-np:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNd6099aca5c36040aab8164a3e9b39a1b
sio:SIO_000628
miriam-gene:4397
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_provenance
{
dgn-np:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_assertion
dcterms:description
"[Several of the regions that showed evidence for nominal significance (P < .05) in our data set had previously been implicated in RA (D16S516 and D17S1301) or in other diseases of an autoimmune nature, including systemic lupus erythematosus (D1S235), inflammatory bowel disease (D4S1647, D5S1462, and D16S516), multiple sclerosis (D12S1052), and ankylosing spondylitis (D16S516).]. 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:11254450
;
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:NP549707.RAwiSZTyhOri475PxMeLMT1dKCiDJLjVLbChw7rusMirI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
}