@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo
> .
@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/
> .
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_head
{
this:
np:hasAssertion
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_assertion
;
np:hasProvenance
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_assertion
a
np:Assertion
.
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_provenance
a
np:Provenance
.
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN25a246ba016680a6338cc58c13399e90
sio:SIO_000628
miriam-gene:6647
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_provenance
{
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_assertion
dcterms:description
"[Mutations in the genes Minibrain and SOD1 have been implicated in the development of learning defects in Down syndrome and many new genes from human chromosome 21 are being cloned, which should result in the genesis of other models that phenocopy one or more pathologies of the syndrome.]. 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:9690992
;
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 .
}
dgn-np:NP1401057.RAyXAJmtgjTia91IKbuTGtMJa_XKPk9xaTKhi33IleLQo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:21+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}