@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM
> .
@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:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_head
{
this:
np:hasAssertion
dgn-np:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_assertion
;
np:hasProvenance
dgn-np:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_provenance
;
np:hasPublicationInfo
dgn-np:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_assertion
a
np:Assertion
.
dgn-np:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_provenance
a
np:Provenance
.
dgn-np:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_assertion
{
miriam-gene:27319
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN1ef700bc7af503d642d383310a077b3d
sio:SIO_000628
miriam-gene:27319
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_provenance
{
dgn-np:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_assertion
dcterms:description
"[The integrin beta3 (ITGB3) and serotonin transporter (SLC6A4) genes were both recently identified as male quantitative trait loci (QTLs) for serotonin levels and alleles of each have been associated with autism.]. 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:16721604
;
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:NP680836.RA6rip_ftQJcKI-HJyY9P6FyxqKIn8jSPps6eBL9aMbTM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:50+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" .
}