@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc
> .
@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:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_head
{
this:
np:hasAssertion
dgn-np:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_assertion
;
np:hasProvenance
dgn-np:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_provenance
;
np:hasPublicationInfo
dgn-np:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_assertion
a
np:Assertion
.
dgn-np:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_provenance
a
np:Provenance
.
dgn-np:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_assertion
{
miriam-gene:2539
a
ncit:C16612
.
lld:C0017758
a
ncit:C7057
.
dgn-gda:DGN763828159e9f4a45f94a2d48d227b7fa
sio:SIO_000628
miriam-gene:2539
,
lld:C0017758
;
a
sio:SIO_001122
.
}
dgn-np:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_provenance
{
dgn-np:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_assertion
dcterms:description
"[DHPLC is of great advantage to screen the G6PD deficient variants with accuracy, convenience, automation and less cost, and significantly to identify the female heterozygote and clinical type IV individuals with G6PD deficiency.]. 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:16331553
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43809.RAQvGLZ72m5Pu-wLukNMeHkpMsa4eHvGxM3VCsHoaI1Dc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}