@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI
> .
@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:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_head
{
this:
np:hasAssertion
dgn-np:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_assertion
;
np:hasProvenance
dgn-np:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_assertion
a
np:Assertion
.
dgn-np:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_provenance
a
np:Provenance
.
dgn-np:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0006370
a
ncit:C7057
.
dgn-gda:DGNd198816675cf482422743eea2182e9eb
sio:SIO_000628
miriam-gene:6532
,
lld:C0006370
;
a
sio:SIO_001122
.
}
dgn-np:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_provenance
{
dgn-np:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_assertion
dcterms:description
"[In our sample of normal-eater controls and purging type bulimics, regardless of whether or not the BN patients had suffered prior AN episodes, no differences were found considering the frequencies of genotypes, alleles or haplotypes of both polymorphic regions of the 5-HTT gene.]. 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:14625025
;
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:NP51518.RAOktl-qz8ETiB8OP9j4puXGoMQF-UCyfHzCC8FHH1gYI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}