@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ
> .
@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/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_assertion
a
np:Assertion
.
dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_provenance
a
np:Provenance
.
dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:1827
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGNbc0995dda2256781ae83224445f8782d
sio:SIO_000628
miriam-gene:1827
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_provenance
{
dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_assertion
dcterms:description
"[These results, combined with our data showing that the same biochemical signaling pathway is altered in human DS fetal brain tissue overexpressing DSCR1, suggest that alteration of DSCR1 expression could contribute to mental retardation in DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:14668437
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:57+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
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