@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg
> .
@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:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_head
{
this:
np:hasAssertion
dgn-np:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_assertion
;
np:hasProvenance
dgn-np:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_provenance
;
np:hasPublicationInfo
dgn-np:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_assertion
a
np:Assertion
.
dgn-np:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_provenance
a
np:Provenance
.
dgn-np:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_assertion
{
miriam-gene:4544
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN5060878d14b153c637cfc2826aa9aa6a
sio:SIO_000628
miriam-gene:4544
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_provenance
{
dgn-np:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_assertion
dcterms:description
"[In this study, we investigated whether single nucleotide polymorphisms (SNPs) in the promoter region of the melatonin receptor genes (MTNR1A and MTNR1B) were associated with schizophrenia and with sleep problems such as insomnia and hypersomnia in schizophrenia patients.]. 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:21526376
;
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:NP701362.RA_VzSVbEoHmOrx-1vH0fFy0fCwAvT-JCj2Mp7LH3SuOg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}