@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I
> .
@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 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:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_head
{
this:
np:hasAssertion
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_assertion
;
np:hasProvenance
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_provenance
;
np:hasPublicationInfo
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_assertion
a
np:Assertion
.
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_provenance
a
np:Provenance
.
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_assertion
{
miriam-gene:3356
a
ncit:C16612
.
lld:C1269683
a
ncit:C7057
.
dgn-gda:DGN87b9723c9ba8412cd715b5073f09cbef
sio:SIO_000628
miriam-gene:3356
,
lld:C1269683
;
a
sio:SIO_001122
.
}
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_provenance
{
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_assertion
dct:description
"[Although these data should be interpreted cautiously due to the small sample size, these results implicate TPH1 and SLC6A4 in general response, and HTR2A, TPH2, and MAOA in the specificity of response to fluoxetine. Intriguingly, we observe that a number of the less frequent alleles of many of the SNP markers were associated with the nonresponse and nonspecific phenotypes.]. 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:15052272
;
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:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:27+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}