@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc
> .
@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:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_head
{
this:
np:hasAssertion
dgn-np:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_assertion
;
np:hasProvenance
dgn-np:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_provenance
;
np:hasPublicationInfo
dgn-np:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_assertion
a
np:Assertion
.
dgn-np:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_provenance
a
np:Provenance
.
dgn-np:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_assertion
{
miriam-gene:9690
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN394983a33d47e0edacf23c3fbc1d0b6f
sio:SIO_000628
miriam-gene:9690
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_provenance
{
dgn-np:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_assertion
dcterms:description
"[The rs3802122 and rs6979947 polymorphisms were significantly associated with the risk of AIA. However, further studies are required to establish the underlying mechanism by which UBE3C and its polymorphisms affect the risk of AIA.]. 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:20934631
;
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:NP90632.RAHaq4zsGSzNuu3iOfeyobL2tsnOwARviv-pVSSMvuLSc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}