@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ
> .
@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:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_head
{
this:
np:hasAssertion
dgn-np:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_assertion
;
np:hasProvenance
dgn-np:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_assertion
a
np:Assertion
.
dgn-np:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_provenance
a
np:Provenance
.
dgn-np:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_assertion
{
miriam-gene:54658
a
ncit:C16612
.
lld:C2939465
a
ncit:C7057
.
dgn-gda:DGN831c096d16d31852c50b49e4b2b1eeea
sio:SIO_000628
miriam-gene:54658
,
lld:C2939465
;
a
sio:SIO_001121
.
}
dgn-np:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_provenance
{
dgn-np:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_assertion
dcterms:description
"[PCR and restriction fragment length polymorphism were used to analyze the promoter area and nucleotides 211, 686, 1,091, and 1,456 of the UGT1A1 gene for all subjects and the gene variants for thalassemia and 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:16237771
;
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:NP564534.RA4UUfYHc7tVKU2JAINppHXSleT_X-jIMwWCj6fWz_1iQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}