@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y
> .
@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:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_head
{
this:
np:hasAssertion
dgn-np:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_assertion
;
np:hasProvenance
dgn-np:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_assertion
a
np:Assertion
.
dgn-np:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_provenance
a
np:Provenance
.
dgn-np:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_assertion
{
miriam-gene:283120
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGNa6acd4814eb20506e72f63479f8e375b
sio:SIO_000628
miriam-gene:283120
,
lld:C0005684
;
a
sio:SIO_001121
.
}
dgn-np:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_provenance
{
dgn-np:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_assertion
dcterms:description
"[Loss of methylation imprinting of H19 is linked to hypomethylation of the paternal allele in human bladder cancer, unlike the situation in Wilms' tumor and colon cancer where the maternal allele becomes hypermethylated.]. 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:11726548
;
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:NP812260.RAk2qTQ-THMeEhl7ipW0NwVJhb_e7zh3Vh7yKzsGzfY0Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}