@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg
> .
@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:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_head
{
this:
np:hasAssertion
dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_assertion
;
np:hasProvenance
dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_provenance
;
np:hasPublicationInfo
dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_assertion
a
np:Assertion
.
dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_provenance
a
np:Provenance
.
dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_assertion
{
miriam-gene:4128
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNd74815761369502c1de67a313482f84c
sio:SIO_000628
miriam-gene:4128
,
lld:C0004352
;
a
sio:SIO_001122
.
}
dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_provenance
{
dgn-np:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_assertion
dcterms:description
"[Suggested mechanisms for hyperserotonemia in autism have been increased synthesis of serotonin (5HT) by tryptophan hydroxylase (TPH), increased uptake into platelets through 5HT transporter (5HTt), diminished release from platelets through 5HT2A receptor (5HT2Ar) and decreased metabolism by monoamine oxydase (MAOA).]. 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:18405062
;
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:NP55024.RA2saFndTGKnRkNbLDD5uy5iR3tJR0MPBX7DDt05nOhxg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}