@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_head
{
this:
np:hasAssertion
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_assertion
;
np:hasProvenance
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_assertion
a
np:Assertion
.
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_provenance
a
np:Provenance
.
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_assertion
{
miriam-gene:3663
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNa818b505a2ba98d3df54ac79175dede8
sio:SIO_000628
miriam-gene:3663
,
lld:C0003873
;
a
sio:SIO_001122
.
}
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_provenance
{
dgn-np:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_assertion
dcterms:description
"[The majority of RA risk alleles previously validated for RA patients of European ancestry showed similar ORs in our population of African Americans with RA. Furthermore, the aggregate GRS supports the hypothesis that these SNPs are risk alleles for RA in ]. 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:21120996
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP87006.RAL2v-UaK4Ax9oxRWp0douH3Z0KPRX0HV1n9Q5wxeI6qQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:28+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}