@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY
> .
@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:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_head
{
this:
np:hasAssertion
dgn-np:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_assertion
;
np:hasProvenance
dgn-np:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_provenance
;
np:hasPublicationInfo
dgn-np:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_assertion
a
np:Assertion
.
dgn-np:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_provenance
a
np:Provenance
.
dgn-np:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_assertion
{
miriam-gene:1666
a
ncit:C16612
.
lld:C0850497
a
ncit:C7057
.
dgn-gda:DGN7331b155301b9c62ad5904c24a09c4f4
sio:SIO_000628
miriam-gene:1666
,
lld:C0850497
;
a
sio:SIO_001121
.
}
dgn-np:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_provenance
{
dgn-np:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_assertion
dcterms:description
"[Chronic granulomatous disease (CGD) is an immune deficiency syndrome caused by defects in the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, the enzyme that generates reactive oxygen species (ROS) in phagocytizing leukocytes.]. 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:21604087
;
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:NP296835.RAelli4zm6GvhjwxdBIXqEvNKYPsKMaAnVFHf53BGLFmY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}