@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo
> .
@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:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_head
{
this:
np:hasAssertion
dgn-np:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_assertion
;
np:hasProvenance
dgn-np:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_provenance
;
np:hasPublicationInfo
dgn-np:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_assertion
a
np:Assertion
.
dgn-np:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_provenance
a
np:Provenance
.
dgn-np:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_assertion
{
miriam-gene:4353
a
ncit:C16612
.
lld:C0018203
a
ncit:C7057
.
dgn-gda:DGNe6c353f0806a5190aacf28f997a0e1f6
sio:SIO_000628
miriam-gene:4353
,
lld:C0018203
;
a
sio:SIO_001121
.
}
dgn-np:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_provenance
{
dgn-np:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_assertion
dcterms:description
"[Although the contribution of myeloperoxidase to the chemiluminescence assay has been noted, the possible diagnostic confusion between chronic granulomatous disease of childhood (which is rare and severe) and myeloperoxidase deficiency (which is common and of little clinical consequence) has not been stressed.]. 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:6297833
;
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:NP825854.RAPVkbWegtuidywh5SUONuft21eY_8R-vK3v-KS9JwLFo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}