@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_head
{
this:
np:hasAssertion
dgn-np:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_assertion
a
np:Assertion
.
dgn-np:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_provenance
a
np:Provenance
.
dgn-np:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_assertion
{
miriam-gene:3275
a
ncit:C16612
.
lld:C0679466
a
ncit:C7057
.
dgn-gda:DGNf3628643c604f49a4d76d35a4da58c2a
sio:SIO_000628
miriam-gene:3275
,
lld:C0679466
;
a
sio:SIO_001121
.
}
dgn-np:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_provenance
{
dgn-np:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_assertion
dcterms:description
"[Thus we conclude that the genes conserved between mouse and human, found in the most telomeric part of Hsa21, and trisomic in Tc1, are not contributing to the major Tc1 phenotypes, suggesting that the Cstb-Prmt2 region is not playing a major role in locomotor and cognitive deficits found in DS.]. 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:21047530
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP465613.RAxuC_zehZsz0FdIImZ-eHIoYVhAyVCEG2VKoSkTAR5co130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:14+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
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;
pav:authoredBy
<
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> , <
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> , <
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
}