@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_assertion
;
np:hasProvenance
dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_provenance
;
np:hasPublicationInfo
dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_assertion
a
np:Assertion
.
dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_provenance
a
np:Provenance
.
dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0019829
a
ncit:C7057
.
dgn-gda:DGN0c51e8a9daea67b23ee3dd10f218b397
sio:SIO_000628
miriam-gene:472
,
lld:C0019829
;
a
sio:SIO_001121
.
}
dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_provenance
{
dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_assertion
dcterms:description
"[The frequency of ATM variants was analyzed in the total group of 64 cases of HD and compared to allele frequencies in 128 ethnically matched controls from the same geographical 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:12473594
;
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:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:31+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" .
}