@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk
> .
@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:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_head
{
this:
np:hasAssertion
dgn-np:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_assertion
;
np:hasProvenance
dgn-np:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_provenance
;
np:hasPublicationInfo
dgn-np:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_assertion
a
np:Assertion
.
dgn-np:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_provenance
a
np:Provenance
.
dgn-np:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_assertion
{
miriam-gene:10518
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGN357b075c427c4c82ed5085ce3841eb23
sio:SIO_000628
miriam-gene:10518
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_provenance
{
dgn-np:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_assertion
dcterms:description
"[Two other 11p15.5 loci, the linked and oppositely imprinted H19 and IGF2 genes, have been previously implicated in WT pathogenesis, and several of the tumors with persistent KIP2 mRNA expression and absence of KIP2 coding mutations showed full inactivation of H19.]. 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:9311733
;
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:NP851257.RAy18ImJHBxlSCkD13rF8V2G7SPJzTtIItTA2QbQbuxsk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:40+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" .
}