@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y
> .
@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:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_head
{
this:
np:hasAssertion
dgn-np:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_assertion
;
np:hasProvenance
dgn-np:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_assertion
a
np:Assertion
.
dgn-np:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_provenance
a
np:Provenance
.
dgn-np:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_assertion
{
miriam-gene:721
a
ncit:C16612
.
lld:C3280642
a
ncit:C7057
.
dgn-gda:DGN5a64b4aaf0fd63279da6abadcbf458a1
sio:SIO_000628
miriam-gene:721
,
lld:C3280642
;
a
sio:SIO_001121
.
}
dgn-np:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_provenance
{
dgn-np:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_assertion
dcterms:description
"[Moreover, partial C4 deficiency appears to be a common risk factor for the development of systemic lupus erythematosus, with complete C4A deficiency (C4A null) being present in 10 to 15 percent and heterozygous C4A deficiency present in 50 to 80 percent of patients with systemic lupus erythematosus.]. 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:3202107
;
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:NP398425.RAuQp6X6OjTmN_k8zXng1ZDVdQ98sjBhM0jrmEhdWTB-Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:57+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" .
}