@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ
> .
@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:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_head
{
this:
np:hasAssertion
dgn-np:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_assertion
;
np:hasProvenance
dgn-np:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_assertion
a
np:Assertion
.
dgn-np:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_provenance
a
np:Provenance
.
dgn-np:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_assertion
{
miriam-gene:3251
a
ncit:C16612
.
lld:C0023374
a
ncit:C7057
.
dgn-gda:DGN2959c05e66f00a280364c6f622d25d36
sio:SIO_000628
miriam-gene:3251
,
lld:C0023374
;
a
sio:SIO_001121
.
}
dgn-np:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_provenance
{
dgn-np:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_assertion
dcterms:description
"[We characterized five unrelated patients with HPRT deficiency to understand the spectrum of molecular defects using Southern and Northern blot, polymerase chain amplification of HPRT mRNA and DNA sequencing, and oligonucleotide hybridization analysis of the HPRT gene.]. 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:2572141
;
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:NP266024.RApiC3QmTKjcVvTGjcshnIs32p07nAU0dIT-yUMJ9OqWQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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" .
}