@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ
> .
@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:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_head
{
this:
np:hasAssertion
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_assertion
;
np:hasProvenance
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_assertion
a
np:Assertion
.
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_provenance
a
np:Provenance
.
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_assertion
{
miriam-gene:1827
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN3167c3123cd5f38c81d32d1f1f6f0a45
sio:SIO_000628
miriam-gene:1827
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_provenance
{
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_assertion
dcterms:description
"[Furthermore, the map enabled us to present evidence against the necessary involvement of other loci as well as specific hypotheses that have been put forward in relation to the etiology of DS-i.e., the presence of a single DS consensus region and the sufficiency of DSCR1 and DYRK1A, or APP, in causing several severe DS phenotypes.]. 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:19597142
;
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:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:21+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: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" .
}