@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q
> .
@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:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_head
{
this:
np:hasAssertion
dgn-np:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_assertion
;
np:hasProvenance
dgn-np:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_assertion
a
np:Assertion
.
dgn-np:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_provenance
a
np:Provenance
.
dgn-np:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_assertion
{
miriam-gene:1827
a
ncit:C16612
.
lld:C0741916
a
ncit:C7057
.
dgn-gda:DGN6f310fcbafdc65f54a5382a0bd1a7041
sio:SIO_000628
miriam-gene:1827
,
lld:C0741916
;
a
sio:SIO_001121
.
}
dgn-np:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_provenance
{
dgn-np:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_assertion
dcterms:description
"[Structural characteristics, together with its particular expression in brain and heart, encourage us to suggest that the overexpression of DSCR1 may be involved in the pathogenesis of Down syndrome, in particular mental retardation and/or cardiac defects.]. 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:8595418
;
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:NP379152.RAjfY5Yv1XnTU4uroqCk4yYDmUjGjHt9JwtmgrrhlUM_Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:44+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" .
}