@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08
> .
@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:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_head
{
this:
np:hasAssertion
dgn-np:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_assertion
;
np:hasProvenance
dgn-np:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_provenance
;
np:hasPublicationInfo
dgn-np:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_assertion
a
np:Assertion
.
dgn-np:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_provenance
a
np:Provenance
.
dgn-np:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGN1d6094b8d5b7b177a3bf327b279b0c60
sio:SIO_000628
miriam-gene:1499
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_provenance
{
dgn-np:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_assertion
dcterms:description
"[We found that abnormalities of WTX and CTNNB1 were mutually exclusive, and that although CTNNB1 mutation was frequent in WTs with WT1 abnormality, but rare in WTs without, the incidences of WTX abnormality were similar between WTs with or without WT1 abnormality.]. 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:22409817
;
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:NP512276.RAz_zzs89nqqNLfMloRHv9htvAPLRCZsMX5W0QH5fGu08130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}