@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc
> .
@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:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_head
{
this:
np:hasAssertion
dgn-np:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_assertion
;
np:hasProvenance
dgn-np:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_provenance
;
np:hasPublicationInfo
dgn-np:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_assertion
a
np:Assertion
.
dgn-np:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_provenance
a
np:Provenance
.
dgn-np:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_assertion
{
miriam-gene:9568
a
ncit:C16612
.
lld:C0028043
a
ncit:C7057
.
dgn-gda:DGN9b419bc907e009e5f16342685ed3bbf4
sio:SIO_000628
miriam-gene:9568
,
lld:C0028043
;
a
sio:SIO_001121
.
}
dgn-np:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_provenance
{
dgn-np:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_assertion
dcterms:description
"[The variants of GABBR1 and GABBR2 are significantly associated with ND, and the involvement of GABBR1 is most likely through its interaction with GABBR2, whereas GABBR2 polymorphisms directly alter susceptibility to ND.]. 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:19763258
;
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:NP596112.RAKO-wZJ30O_7TIrgWzsjJCRF1rJK1qrsdmn94XgFPxPc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:58+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" .
}