@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo
> .
@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:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_head
{
this:
np:hasAssertion
dgn-np:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_assertion
;
np:hasProvenance
dgn-np:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_provenance
;
np:hasPublicationInfo
dgn-np:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_assertion
a
np:Assertion
.
dgn-np:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_provenance
a
np:Provenance
.
dgn-np:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_assertion
{
miriam-gene:1378
a
ncit:C16612
.
lld:C0014060
a
ncit:C7057
.
dgn-gda:DGN8a5abe4d6dd3f1fce2ada80405482562
sio:SIO_000628
miriam-gene:1378
,
lld:C0014060
;
a
sio:SIO_001121
.
}
dgn-np:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_provenance
{
dgn-np:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_assertion
dcterms:description
"[These data provide further evidence that there are enhanced extracellular mechanisms for the removal of CR1 from erythrocytes of SLE patients and do not support the hypothesis that inherited variation in CR1 expression on erythrocytes increases disease susceptibility to SLE.]. 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:2899464
;
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:NP732026.RArlyUJr4wqzm1_fRZ8epzr-Kkmx8yRmhVN-iJG5DSBgo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:24+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" .
}