@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms
> .
@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:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_head
{
this:
np:hasAssertion
dgn-np:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_assertion
;
np:hasProvenance
dgn-np:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_provenance
;
np:hasPublicationInfo
dgn-np:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_assertion
a
np:Assertion
.
dgn-np:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_provenance
a
np:Provenance
.
dgn-np:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_assertion
{
miriam-gene:50506
a
ncit:C16612
.
lld:C0018203
a
ncit:C7057
.
dgn-gda:DGNb1c01bd8e13519b4b363d8a794baf7a7
sio:SIO_000628
miriam-gene:50506
,
lld:C0018203
;
a
sio:SIO_001121
.
}
dgn-np:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_provenance
{
dgn-np:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_assertion
dcterms:description
"[Chronic granulomatous disease (CGD) is an inherited disorder of the nicotinamide adenine dinucleotide phosphate oxidase that leads to defective production of microbicidal superoxide and other oxidative radicals, resulting in increased susceptibility to invasive infections, especially those due to fungi.]. 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:21367720
;
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:NP761080.RAvvhq35_BE-1VHex6LO_G4GbPRfqyGoczcDDfdlShrms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}