@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU
> .
@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:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_head
{
this:
np:hasAssertion
dgn-np:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_assertion
;
np:hasProvenance
dgn-np:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_provenance
;
np:hasPublicationInfo
dgn-np:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_assertion
a
np:Assertion
.
dgn-np:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_provenance
a
np:Provenance
.
dgn-np:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_assertion
{
miriam-gene:406
a
ncit:C16612
.
lld:C0085207
a
ncit:C7057
.
dgn-gda:DGN667bbe7049126ca243818fa2dd7bfb40
sio:SIO_000628
miriam-gene:406
,
lld:C0085207
;
a
sio:SIO_001121
.
}
dgn-np:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_provenance
{
dgn-np:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_assertion
dcterms:description
"[These data document for the first time that the expression of BMAL1, PER3, PPARD and CRY2 genes is altered in GDM compared to normal pregnant women and support the notion that deranged expression of clock genes may play a pathogenic role in GDM.]. 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:23323702
;
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:NP541231.RAPqgfFcz4SVDogOMlNyIJKnwWsxvFOXadnvjs6GgWdvU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:26+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" .
}