@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E
> .
@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:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_head
{
this:
np:hasAssertion
dgn-np:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_assertion
;
np:hasProvenance
dgn-np:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_provenance
;
np:hasPublicationInfo
dgn-np:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_assertion
a
np:Assertion
.
dgn-np:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_provenance
a
np:Provenance
.
dgn-np:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_assertion
{
miriam-gene:10950
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNf5cf05ca8f1c83e1cf320754aed1b0f9
sio:SIO_000628
miriam-gene:10950
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_provenance
{
dgn-np:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_assertion
dcterms:description
"[We have therefore tested the hypothesis that in SLE C4 null alleles are directly involved by examining (1) whether all or only some AH bearing C4 null alleles are increased, (2) whether C4 null is increased in all racial groups examined, and (3) whether C4 null is associated with the presence of antinuclear antibodies (ANA) in the absence of 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:1757937
;
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:NP475690.RAV5i-ySmjMH7ILr5HWnAl0oBs7W4tZYqxfjbmZuZlG_E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}