@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0
> .
@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:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_head
{
this:
np:hasAssertion
dgn-np:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_assertion
;
np:hasProvenance
dgn-np:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_provenance
;
np:hasPublicationInfo
dgn-np:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_assertion
a
np:Assertion
.
dgn-np:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_provenance
a
np:Provenance
.
dgn-np:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_assertion
{
miriam-gene:8863
a
ncit:C16612
.
lld:C0037317
a
ncit:C7057
.
dgn-gda:DGN10bbe734dd2c88a818516bce29a1833f
sio:SIO_000628
miriam-gene:8863
,
lld:C0037317
;
a
sio:SIO_001121
.
}
dgn-np:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_provenance
{
dgn-np:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_assertion
dcterms:description
"[Circadian rhythm-related sleep disorders have also been associated with mutations and polymorphisms in clock genes, with the advanced type cosegrating in an autosomal dominant inheritance pattern with mutations in the genes PER2 and CSNK1D, and the delayed type associating without discernible Mendelian inheritance with polymorphisms in CLOCK and PER3.]. 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:19147940
;
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:NP617366.RA4w5toSUZoGeWxMnSU5a4KGEawRdl5GaSVowFvBm2Uj0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}