@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E
> .
@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:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_head
{
this:
np:hasAssertion
dgn-np:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_assertion
;
np:hasProvenance
dgn-np:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_assertion
a
np:Assertion
.
dgn-np:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_provenance
a
np:Provenance
.
dgn-np:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_assertion
{
miriam-gene:283120
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNf3bfe4cc6fa3a0ccd1cdc563bbaa2c13
sio:SIO_000628
miriam-gene:283120
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_provenance
{
dgn-np:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_assertion
dcterms:description
"[Together with the previous reports on altered genomic imprinting of IGF2 and H19 in embryonal lesions such as Wilms tumors as well as in lung cancers, the results suggest that perturbations of imprinting status occur as locus and tumor-type specific events in the development of human cancers.]. 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:8622877
;
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:NP225594.RATeVtxCuAP0XVgTjfKqAMYRwjKL3fSXDxZSOs9DYBt3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}