@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg
> .
@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:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_head
{
this:
np:hasAssertion
dgn-np:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_assertion
;
np:hasProvenance
dgn-np:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_provenance
;
np:hasPublicationInfo
dgn-np:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_assertion
a
np:Assertion
.
dgn-np:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_provenance
a
np:Provenance
.
dgn-np:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_assertion
{
miriam-gene:5423
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN2a1f457f536a8fba9112a179d0def816
sio:SIO_000628
miriam-gene:5423
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_provenance
{
dgn-np:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_assertion
dcterms:description
"[Like that seen in the DNA polymerase beta heterozygous mouse, the aging phenotype of Down syndrome is subtle, unlike the aging phenotypes seen in the classical progeroid syndromes and mouse models of aging.]. 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:22019846
;
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:NP464334.RA8qgmGqcP8uqhp0LX7ZLN8HU07GU0K4gKzysPnNNNMwg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:36+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" .
}