@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y
> .
@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:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_head
{
this:
np:hasAssertion
dgn-np:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_assertion
;
np:hasProvenance
dgn-np:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_assertion
a
np:Assertion
.
dgn-np:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_provenance
a
np:Provenance
.
dgn-np:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_assertion
{
miriam-gene:1786
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN2ce26e2f28aea6e0402b6853679a5a43
sio:SIO_000628
miriam-gene:1786
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_provenance
{
dgn-np:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_assertion
dcterms:description
"[Rapid amplification of cDNA ends (RACE) mapping revealed that the transcriptional start site of BORIS in human testis, DNMT deficient human cancer cells, and human epithelial ovarian cancer (EOC) tissues, is similar and lies within the 5' CpG island.]. 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:18095639
;
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:NP164788.RAZNX4tWa8KAq11Ot_0Ba0i9ysIRP8j_1z2e0qZeLeZ7Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}