@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684154.RAnMeP7wRz_FYVCo5I7KTtBItXUWdxHwBi39zn0yEYqio
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP684154.RAnMeP7wRz_FYVCo5I7KTtBItXUWdxHwBi39zn0yEYqio130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP684154.RAnMeP7wRz_FYVCo5I7KTtBItXUWdxHwBi39zn0yEYqio130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP684154.RAnMeP7wRz_FYVCo5I7KTtBItXUWdxHwBi39zn0yEYqio130_assertion
a
np:Assertion
.
dgn-np:NP684154.RAnMeP7wRz_FYVCo5I7KTtBItXUWdxHwBi39zn0yEYqio130_provenance
a
np:Provenance
.
dgn-np:NP684154.RAnMeP7wRz_FYVCo5I7KTtBItXUWdxHwBi39zn0yEYqio130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:83853
a
ncit:C16612
.
lld:C0553662
a
ncit:C7057
.
dgn-gda:DGNfe6ad74ff3687d69055cae688641338f
sio:SIO_000628
miriam-gene:83853
,
lld:C0553662
;
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.
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dgn-np:NP684154.RAnMeP7wRz_FYVCo5I7KTtBItXUWdxHwBi39zn0yEYqio130_provenance
{
dgn-np:NP684154.RAnMeP7wRz_FYVCo5I7KTtBItXUWdxHwBi39zn0yEYqio130_assertion
dcterms:description
"[To investigate the clinical phenotypes and demographic characteristics of 183 affected sibling pairs (ASPs) with juvenile rheumatoid arthritis (JRA) and to determine whether there are differences between the clinical phenotypes of the ASP cohort compared with patients with sporadic disease and whether there is greater sharing of specific clinical features within versus between sibpairs.]. 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:15188369
;
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:NP684154.RAnMeP7wRz_FYVCo5I7KTtBItXUWdxHwBi39zn0yEYqio130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+02:00"^^
xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
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> , <
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> , <
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> ;
pav:createdBy
<
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pav:version
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