@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U
> .
@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:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_head
{
this:
np:hasAssertion
dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_assertion
;
np:hasProvenance
dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_provenance
;
np:hasPublicationInfo
dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_assertion
a
np:Assertion
.
dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_provenance
a
np:Provenance
.
dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_assertion
{
miriam-gene:966
a
ncit:C16612
.
lld:C2676767
a
ncit:C7057
.
dgn-gda:DGN32e8af242622ba202f5017c5af5f35d3
sio:SIO_000628
miriam-gene:966
,
lld:C2676767
;
a
sio:SIO_001121
.
}
dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_provenance
{
dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_assertion
dcterms:description
"[CD59 deficiency is a common finding in RBCs and WBCs in patients with chronic hemolysis suffering from paroxysmal nocturnal hemoglobinuria in which the acquired mutation in the PIGA gene leads to membrane loss of glycosylphosphatidylinositol-anchored membrane proteins, including CD59.]. 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:23149847
;
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:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+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" .
}