@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0
> .
@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:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_head
{
this:
np:hasAssertion
dgn-np:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_assertion
;
np:hasProvenance
dgn-np:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_provenance
;
np:hasPublicationInfo
dgn-np:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_assertion
a
np:Assertion
.
dgn-np:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_provenance
a
np:Provenance
.
dgn-np:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_assertion
{
miriam-gene:720
a
ncit:C16612
.
lld:C0086445
a
ncit:C7057
.
dgn-gda:DGN1948a52b3567bb0d8c54866f6e26e1fc
sio:SIO_000628
miriam-gene:720
,
lld:C0086445
;
a
sio:SIO_001121
.
}
dgn-np:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_provenance
{
dgn-np:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_assertion
dcterms:description
"[To clarify whether C4A deletion is an independent risk factor for IMN or is increased secondarily to the Caucasoid HLA A1, B8, DR3 extended haplotype, we examined the frequency of C4A deletion in Japanese patients, in whom the disease is associated with another HLA haplotype (DR2-DQw1).]. 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:1360552
;
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:NP462117.RAtYzo2AOouwMsaDMrk8nSzC8hhm357_R1oPdBBOfUhp0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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" .
}