@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M
> .
@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:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_head
{
this:
np:hasAssertion
dgn-np:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_assertion
;
np:hasProvenance
dgn-np:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_provenance
;
np:hasPublicationInfo
dgn-np:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_assertion
a
np:Assertion
.
dgn-np:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_provenance
a
np:Provenance
.
dgn-np:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_assertion
{
miriam-gene:847
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGN69be697977368b44e1a5d1ba539a9e47
sio:SIO_000628
miriam-gene:847
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_provenance
{
dgn-np:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_assertion
dcterms:description
"[We studied the RBC catalase levels in individuals without detectable chromosomal abnormalities but with aniridia, Wilm's tumor, and the combination of aniridia and Wilms' tumor, to determine whether catalase levels might provide evidence for a submicroscopic chromosomal deletion in the 11p13 region.]. 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:6273073
;
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:NP835641.RAc1Fjod1qhyq1EVVG6cIGBMC1EM0yETB6GaxB4M_Yh9M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:31+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" .
}