@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c
> .
@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:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_head
{
this:
np:hasAssertion
dgn-np:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_assertion
;
np:hasProvenance
dgn-np:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_provenance
;
np:hasPublicationInfo
dgn-np:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_assertion
a
np:Assertion
.
dgn-np:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_provenance
a
np:Provenance
.
dgn-np:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_assertion
{
miriam-gene:1734
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGNec8f56ffa70e616efdc7b1035b4ba161
sio:SIO_000628
miriam-gene:1734
,
lld:C0005586
;
a
sio:SIO_001122
.
}
dgn-np:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_provenance
{
dgn-np:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_assertion
dcterms:description
"[Data generated from this study supported our hypothesis that genetic variations of the DIO2 gene were associated with BPAD and suggested further consideration on the possible involvement of these functionally active variants in the pathophysiology of BPAD.]. 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:19427350
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP75957.RAP-mwQXG2Coz_U3tdPz94L29A7WM91QTzX3qOQzJ-u2c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:37+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" .
}