@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0
> .
@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:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_head
{
this:
np:hasAssertion
dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_assertion
;
np:hasProvenance
dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_provenance
;
np:hasPublicationInfo
dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_assertion
a
np:Assertion
.
dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_provenance
a
np:Provenance
.
dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN84832cf3dc340248ed52b94c95e1d94e
sio:SIO_000628
miriam-gene:1636
,
lld:C0024141
;
a
sio:SIO_001122
.
}
dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_provenance
{
dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_assertion
dcterms:description
"[Taken together, the I/D polymorphisms of ACE gene did not affect susceptibility of SLE, lupus nephritis and the vascular manifestations, including Raynaud's phenomenon, in Korean SLE patients, although the DD genotype was negatively associated with Raynaud's phenomenon among SLE 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:12043886
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}