@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ
> .
@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:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_head
{
this:
np:hasAssertion
dgn-np:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_assertion
;
np:hasProvenance
dgn-np:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_assertion
a
np:Assertion
.
dgn-np:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_provenance
a
np:Provenance
.
dgn-np:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_assertion
{
miriam-gene:6667
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN562ada2c6bc1926f946ff404f9d31a8f
sio:SIO_000628
miriam-gene:6667
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_provenance
{
dgn-np:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_assertion
dcterms:description
"[Among genes that were highly-represented in these enriched pathways, we found indications of coordinated relationships, including one large gene set that is subject to regulation by the SP1 transcription factor, and another set that displays co-localized expression in normal brain tissue along with known AD risk genes.]. 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:22865056
;
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:NP345536.RAvflWfHu563K5LXqr415yUil8CpOYfmR64S0eVY-MDWQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}