@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_head
{
this:
np:hasAssertion
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_assertion
;
np:hasProvenance
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_assertion
a
np:Assertion
.
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_provenance
a
np:Provenance
.
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_assertion
{
miriam-gene:1536
a
ncit:C16612
.
lld:C0018203
a
ncit:C7057
.
dgn-gda:DGN6d825a14c9c2678840e6dba8b9f2cb7b
sio:SIO_000628
miriam-gene:1536
,
lld:C0018203
;
a
sio:SIO_001121
.
}
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_provenance
{
dgn-np:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_assertion
dcterms:description
"[X-Linked (XL) CGD results from a mutation in the CYBB gene encoding the gp91phox subunit, while autosomal recessive (AR) CGD is associated with mutations in one of the NCF1, NCF2 and CYBA genes that encode the p47phox, p67phox and p22phox subunits, respectively.]. 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:16937026
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP566333.RA9AFnbY17q93JSk6oyZL-3XDkCtYl1_Mpn_SOUIlGSsQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:01+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}