@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc
> .
@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:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_head
{
this:
np:hasAssertion
dgn-np:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_assertion
;
np:hasProvenance
dgn-np:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_provenance
;
np:hasPublicationInfo
dgn-np:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_assertion
a
np:Assertion
.
dgn-np:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_provenance
a
np:Provenance
.
dgn-np:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_assertion
{
miriam-gene:5027
a
ncit:C16612
.
lld:C0041696
a
ncit:C7057
.
dgn-gda:DGNd2a2f163702ef19d6fbed9470d7254f2
sio:SIO_000628
miriam-gene:5027
,
lld:C0041696
;
a
sio:SIO_001121
.
}
dgn-np:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_provenance
{
dgn-np:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_assertion
dcterms:description
"[Although genetic findings were not always consistently replicated, several studies demonstrated that single nucleotide polymorphisms (SNPs) in the human P2X7 gene (P2RX7) show significant association with major depressive disorder and bipolar disorder.]. 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:23269209
;
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:NP804766.RAaoluGBrfAeH2ADLoa_uLWvXiDV_wlgk2HnXEelVJLAc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:13+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" .
}