@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP431994.RA_sWYnuWCWzRwABoFWN2_uqRxPVctotAB22Zq32COvIM
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP431994.RA_sWYnuWCWzRwABoFWN2_uqRxPVctotAB22Zq32COvIM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP431994.RA_sWYnuWCWzRwABoFWN2_uqRxPVctotAB22Zq32COvIM130_assertion
a
np:Assertion
.
dgn-np:NP431994.RA_sWYnuWCWzRwABoFWN2_uqRxPVctotAB22Zq32COvIM130_provenance
a
np:Provenance
.
dgn-np:NP431994.RA_sWYnuWCWzRwABoFWN2_uqRxPVctotAB22Zq32COvIM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP431994.RA_sWYnuWCWzRwABoFWN2_uqRxPVctotAB22Zq32COvIM130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN619499f97c0066473d665a1217f8a2cb
sio:SIO_000628
miriam-gene:8170
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP431994.RA_sWYnuWCWzRwABoFWN2_uqRxPVctotAB22Zq32COvIM130_provenance
{
dgn-np:NP431994.RA_sWYnuWCWzRwABoFWN2_uqRxPVctotAB22Zq32COvIM130_assertion
dcterms:description
"[We have tested this hypothesis by sequencing all GRIK2 exons, the exon-flanking sequences and 3'UTR in several individuals who were crucial to demonstrating the modifier effect, as they showed much earlier age at neurological onset than would be expected from the length of their HD CAG mutation.]. 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:16959037
;
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:NP431994.RA_sWYnuWCWzRwABoFWN2_uqRxPVctotAB22Zq32COvIM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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" .
}