@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg
> .
@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:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_head
{
this:
np:hasAssertion
dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_assertion
;
np:hasProvenance
dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_provenance
;
np:hasPublicationInfo
dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_assertion
a
np:Assertion
.
dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_provenance
a
np:Provenance
.
dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_assertion
{
miriam-gene:720
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGN6527d5e30b7c049033f29770f7905e4b
sio:SIO_000628
miriam-gene:720
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_provenance
{
dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_assertion
dcterms:description
"[Interindividual gene copy-number variation (CNV) of complement component C4 and its associated polymorphisms in gene size (long and short) and protein isotypes (C4A and C4B) probably lead to different susceptibilities to autoimmune disease.]. 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:17503323
;
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:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}