@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw
> .
@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:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_head
{
this:
np:hasAssertion
dgn-np:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_assertion
;
np:hasProvenance
dgn-np:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance
;
np:hasPublicationInfo
dgn-np:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_assertion
a
np:Assertion
.
dgn-np:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance
a
np:Provenance
.
dgn-np:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_assertion
{
miriam-gene:25819
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGN51defba9aeaf40851e6a0c7313eac1f3
sio:SIO_000628
miriam-gene:25819
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance
{
dgn-np:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_assertion
dcterms:description
"[In this study, variation screening of the entire coding regions of CCR3 and CCR4 was performed, and possible association with several autoimmune diseases was tested, using the genomic DNA from 304 Japanese healthy individuals and 272 Japanese patients with rheumatic diseases.]. 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:11196669
;
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:NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}