@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM
> .
@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:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_head
{
this:
np:hasAssertion
dgn-np:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_assertion
;
np:hasProvenance
dgn-np:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_provenance
;
np:hasPublicationInfo
dgn-np:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_assertion
a
np:Assertion
.
dgn-np:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_provenance
a
np:Provenance
.
dgn-np:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_assertion
{
miriam-gene:4128
a
ncit:C16612
.
lld:C0700201
a
ncit:C7057
.
dgn-gda:DGN7f8b846fb8d82119d26a3ff6c7d354f1
sio:SIO_000628
miriam-gene:4128
,
lld:C0700201
;
a
sio:SIO_001121
.
}
dgn-np:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_provenance
{
dgn-np:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_assertion
dcterms:description
"[We hypothesized that the risk of sleep disturbance is, at least in part, influenced by the availability of serotonin used for melatonin synthesis secondary to polymorphic variation at the enzyme monoamine oxidase A (MAO-A).]. 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:16944667
;
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:NP666254.RA1z1Ks5wHC5cwQOu5eVlKAvVjoOx1MJPzhh8JooBQWMM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}