@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek
> .
@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:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_head
{
this:
np:hasAssertion
dgn-np:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_assertion
;
np:hasProvenance
dgn-np:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_provenance
;
np:hasPublicationInfo
dgn-np:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_assertion
a
np:Assertion
.
dgn-np:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_provenance
a
np:Provenance
.
dgn-np:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0038644
a
ncit:C7057
.
dgn-gda:DGN65bfb0664666fafc7bbf00c8381a26af
sio:SIO_000628
miriam-gene:6532
,
lld:C0038644
;
a
sio:SIO_001121
.
}
dgn-np:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_provenance
{
dgn-np:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_assertion
dcterms:description
"[Although genes involved in serotonin metabolism have been proposed as risk factors for sudden infant death syndrome (SIDS), the contribution of additional neurotransmitters and genes different from the serotonin transporter (SLC6A4, 5-HTT) has not been investigated.]. 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:18810510
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP298156.RAhWt25PdlV17cqTBr0Ms7NYc3Ghhna6dI2621pd1xRek130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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" .
}