@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY
> .
@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:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_head
{
this:
np:hasAssertion
dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_assertion
;
np:hasProvenance
dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_provenance
;
np:hasPublicationInfo
dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_assertion
a
np:Assertion
.
dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_provenance
a
np:Provenance
.
dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_assertion
{
miriam-gene:1536
a
ncit:C16612
.
lld:C1844376
a
ncit:C7057
.
dgn-gda:DGN10d3b6817ebd4af8e2ad36dea4ef8803
sio:SIO_000628
miriam-gene:1536
,
lld:C1844376
;
a
sio:SIO_001121
.
}
dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_provenance
{
dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_assertion
dcterms:description
"[4) In PMA-stimulated B cells from an X91+ CGD patient in which p22phox was normally expressed and gp91phox was present but lacked five amino acids, translocation of p47phox to the membranes was unaffected, but p67phox and p40phox were poorly translocated, and the production of O2- was greatly reduced with respect to that by normal B cells.]. 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:9794433
;
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:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}