@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo
> .
@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:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_head
{
this:
np:hasAssertion
dgn-np:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_assertion
;
np:hasProvenance
dgn-np:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_provenance
;
np:hasPublicationInfo
dgn-np:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_assertion
a
np:Assertion
.
dgn-np:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_provenance
a
np:Provenance
.
dgn-np:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_assertion
{
miriam-gene:3177
a
ncit:C16612
.
lld:C0851578
a
ncit:C7057
.
dgn-gda:DGNb823e990c277503031b4a74b748db398
sio:SIO_000628
miriam-gene:3177
,
lld:C0851578
;
a
sio:SIO_001122
.
}
dgn-np:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_provenance
{
dgn-np:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_assertion
dcterms:description
"[Our results suggest that compromised adenosine transport due to variation in nucleoside transporter gene SLC29A3 in women, could predispose to depression, and could suggest new directions in treatment research. The shortage of overlapping genes between th]. 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:20392501
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP172833.RAmFn3iE1qXMo9Bq61OQYd_8XI3VGz04gUvsxKIv2BGHo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:05+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" .
}