@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4
> .
@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:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_head
{
this:
np:hasAssertion
dgn-np:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_assertion
;
np:hasProvenance
dgn-np:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_provenance
;
np:hasPublicationInfo
dgn-np:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_assertion
a
np:Assertion
.
dgn-np:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_provenance
a
np:Provenance
.
dgn-np:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_assertion
{
miriam-gene:10125
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNf93c9a796b221e093aca4f00e7bd3de1
sio:SIO_000628
miriam-gene:10125
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_provenance
{
dgn-np:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_assertion
dcterms:description
"[The lack of the normal isoform of RasGRP1 in some SLE patients and the increased prevalence of defective isoforms of RasGRP1 in others raise the possibility that dysregulation of this signaling protein contributes to the development of autoimmunity in a subset of 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:17878389
;
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:NP213279.RAEp4_GXbsEpj84dG47eWhn6XoqA31hXakoL5skywQaD4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:58+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" .
}