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http://rdf.disgenet.org/nanopublications.trig#NP867809.RAurWQOjTRX-eg8gHhCqqN6HqTGDKI5R1MzgBn8ZNxEvU
> .
@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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{
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP867809.RAurWQOjTRX-eg8gHhCqqN6HqTGDKI5R1MzgBn8ZNxEvU130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP867809.RAurWQOjTRX-eg8gHhCqqN6HqTGDKI5R1MzgBn8ZNxEvU130_assertion
a
np:Assertion
.
dgn-np:NP867809.RAurWQOjTRX-eg8gHhCqqN6HqTGDKI5R1MzgBn8ZNxEvU130_provenance
a
np:Provenance
.
dgn-np:NP867809.RAurWQOjTRX-eg8gHhCqqN6HqTGDKI5R1MzgBn8ZNxEvU130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:4858
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGNf802d9ad2aac99312bd71712158a36b9
sio:SIO_000628
miriam-gene:4858
,
lld:C0013080
;
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.
}
dgn-np:NP867809.RAurWQOjTRX-eg8gHhCqqN6HqTGDKI5R1MzgBn8ZNxEvU130_provenance
{
dgn-np:NP867809.RAurWQOjTRX-eg8gHhCqqN6HqTGDKI5R1MzgBn8ZNxEvU130_assertion
dcterms:description
"[Moreover, by having a larger sample size, combining the data from four different tissue and cell types, and using an ANOVA approach, we identified individual genes with significantly altered expression in trisomy 21, some of which showed this dysregulation in a tissue-specific manner.]. 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:16420667
;
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:NP867809.RAurWQOjTRX-eg8gHhCqqN6HqTGDKI5R1MzgBn8ZNxEvU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:50+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
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> , <
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> , <
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> ;
pav:createdBy
<
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pav:version
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"v2.1.0" .
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