@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg
> .
@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:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_head
{
this:
np:hasAssertion
dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_assertion
;
np:hasProvenance
dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_provenance
;
np:hasPublicationInfo
dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_assertion
a
np:Assertion
.
dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_provenance
a
np:Provenance
.
dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_assertion
{
miriam-gene:3362
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN9339f18803628337d2b5e1ad845c63dd
sio:SIO_000628
miriam-gene:3362
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_provenance
{
dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_assertion
dcterms:description
"[These polymorphisms probably do not represent major genetic risk factors of AD. However, further studies including other genetic variants of the serotonergic neurotransmitter system are needed in order to elucidate their role in AD. ]. 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:11692286
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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" .
}