@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw
> .
@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:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_head
{
this:
np:hasAssertion
dgn-np:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_assertion
;
np:hasProvenance
dgn-np:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_provenance
;
np:hasPublicationInfo
dgn-np:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_assertion
a
np:Assertion
.
dgn-np:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_provenance
a
np:Provenance
.
dgn-np:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_assertion
{
miriam-gene:1590
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN8983a1f1015a1d46334518d0bc7a6367
sio:SIO_000628
miriam-gene:1590
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_provenance
{
dgn-np:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_assertion
dcterms:description
"[Since a deletion of the C4A and CyP21A genes is reported to account for C4AQO in patients with systemic lupus erythematosus (SLE) in Caucasians, we studied the restriction fragment length polymorphism (RFLP) of genomic DNA to determine whether similar deletions of the C4A and CyP21A genes occur in Japanese patients with SS.]. 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:1351942
;
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:NP850105.RAeaw7aCv4jPj2J6K36oiGiGYlimnvuXZAPkTjV6cHqNw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:39+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" .
}