@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY
> .
@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:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_head
{
this:
np:hasAssertion
dgn-np:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_assertion
;
np:hasProvenance
dgn-np:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_provenance
;
np:hasPublicationInfo
dgn-np:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_assertion
a
np:Assertion
.
dgn-np:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_provenance
a
np:Provenance
.
dgn-np:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_assertion
{
miriam-gene:2539
a
ncit:C16612
.
lld:C1849472
a
ncit:C7057
.
dgn-gda:DGNdb7ce8e16afce7d93060263b350b5272
sio:SIO_000628
miriam-gene:2539
,
lld:C1849472
;
a
sio:SIO_001121
.
}
dgn-np:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_provenance
{
dgn-np:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_assertion
dcterms:description
"[Since late onset of hemolysis in heterozygous PK-deficient women has been observed in association with pregnancy and the molecular characteristics of the concomitant deficient G6PD enzyme were kinetically favorable, partial PK deficiency is suggested as the major cause of hemolysis in this patient.]. 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:2049468
;
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:NP340813.RAYEqLcJ8qYKrA4aHG1QN_FvbKqC0pOQioB5_5b3-5-dY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:20+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" .
}