@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g
> .
@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:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_head
{
this:
np:hasAssertion
dgn-np:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_assertion
;
np:hasProvenance
dgn-np:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_assertion
a
np:Assertion
.
dgn-np:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_provenance
a
np:Provenance
.
dgn-np:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_assertion
{
miriam-gene:7057
a
ncit:C16612
.
lld:C0022665
a
ncit:C7057
.
dgn-gda:DGNa532729d1333d9921c0894fa4c830153
sio:SIO_000628
miriam-gene:7057
,
lld:C0022665
;
a
sio:SIO_001121
.
}
dgn-np:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_provenance
{
dgn-np:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_assertion
dcterms:description
"[Furthermore, THBS1 CpG sites were found to be specifically hypermethylated in CCSK and, thus, the DNA methylation status of these THBS1 sites alone was sufficient for the distinction of CCSK from other pediatric renal tumors, including Wilms' tumor and CMN.]. 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:23638012
;
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:NP898506.RAIJ-TTrD_khGJKJ2YvkrHR4RuA7ynx9qCFD18dG_el4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:12+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" .
}