@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y
> .
@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:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_head
{
this:
np:hasAssertion
dgn-np:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_assertion
;
np:hasProvenance
dgn-np:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_assertion
a
np:Assertion
.
dgn-np:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_provenance
a
np:Provenance
.
dgn-np:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0011253
a
ncit:C7057
.
dgn-gda:DGN40779885c67ae38b9e421438dbd76558
sio:SIO_000628
miriam-gene:6532
,
lld:C0011253
;
a
sio:SIO_001121
.
}
dgn-np:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_provenance
{
dgn-np:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_assertion
dcterms:description
"[With an increasing number of short (s) alleles of 5-HTTLPR, the scores for delusions, disorganization and negative symptoms were significantly decreasing among subjects having the TPH genotype AA but increasing among subjects having the TPH genotype AC, yielding the highest scores for the combinations AA x ll and AC x ss.]. 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:15627807
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP474728.RA-6rnVtcbabNLZgGbsFt0y0R9XfAxCCSqm-Vv-kKcg9Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:20+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" .
}