@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y
> .
@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:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_head
{
this:
np:hasAssertion
dgn-np:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_assertion
;
np:hasProvenance
dgn-np:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_assertion
a
np:Assertion
.
dgn-np:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_provenance
a
np:Provenance
.
dgn-np:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_assertion
{
miriam-gene:2876
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN529db505b80c535776f5e5f0f50e4457
sio:SIO_000628
miriam-gene:2876
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_provenance
{
dgn-np:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_assertion
dcterms:description
"[Future study of interaction of the GPX1 GCG repeat and other gene polymorphisms such as the MnSOD ALA16 or the GPX1 Pro198Leu polymorphism in this cohort of AD families may shed light in whether the combination of the ALA6 allele with another polymorphism of antioxidant allele contributes to the increased oxidative stress in autism.]. 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:19195803
;
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:NP357623.RA0bS_CwWLJOi8B1HhjBercF5rzuaULdurMxo3aBidL0Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:29+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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dgn-void:disgenetrdf
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"v2.1.0" .
}