@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk
> .
@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:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_head
{
this:
np:hasAssertion
dgn-np:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_assertion
;
np:hasProvenance
dgn-np:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_provenance
;
np:hasPublicationInfo
dgn-np:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_assertion
a
np:Assertion
.
dgn-np:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_provenance
a
np:Provenance
.
dgn-np:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_assertion
{
miriam-gene:1666
a
ncit:C16612
.
lld:C0018203
a
ncit:C7057
.
dgn-gda:DGNbc5b79fbbacd0b1a53c3dcfe24204d3d
sio:SIO_000628
miriam-gene:1666
,
lld:C0018203
;
a
sio:SIO_001121
.
}
dgn-np:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_provenance
{
dgn-np:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_assertion
dcterms:description
"[Chronic granulomatous disease (CGD) is the most common inherited disorder of neutrophil function, is caused by mutations in the reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, and results in recurrent bacterial infections.]. 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:18155283
;
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:NP203373.RA4ucEJfsfJbhhXGqCjwLou2B-PdUkMoFmnMU_1j67Fmk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}