@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY
> .
@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 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:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_head
{
this:
np:hasAssertion
dgn-np:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_assertion
;
np:hasProvenance
dgn-np:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_provenance
;
np:hasPublicationInfo
dgn-np:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_assertion
a
np:Assertion
.
dgn-np:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_provenance
a
np:Provenance
.
dgn-np:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_assertion
{
miriam-gene:2539
a
ncit:C16612
.
lld:C0017758
a
ncit:C7057
.
dgn-gda:DGNa144460c62b0d0fe9462fce3c99db585
sio:SIO_000628
miriam-gene:2539
,
lld:C0017758
;
a
sio:SIO_001122
.
}
dgn-np:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_provenance
{
dgn-np:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_assertion
dct:description
"[By means of mis-matched primers amplified the G6PD gene, the products were 234 bp, 280 bp and 345 bp in length, then restriction enzyme analysis was used to detect the most common Chinese G6PD mutations, 1376 G-->T, 1388 G-->A and 95 A-->G. The results showed that out of the 1,090 samples, 98 G6PD deficiency samples were found.]. 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:15748456
;
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:NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}