@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk
> .
@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:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_head
{
this:
np:hasAssertion
dgn-np:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_assertion
;
np:hasProvenance
dgn-np:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_provenance
;
np:hasPublicationInfo
dgn-np:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_assertion
a
np:Assertion
.
dgn-np:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_provenance
a
np:Provenance
.
dgn-np:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_assertion
{
miriam-gene:4255
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGN3eb34f2d17c14f0ded280886f6c5d905
sio:SIO_000628
miriam-gene:4255
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_provenance
{
dgn-np:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_assertion
dcterms:description
"[These findings suggest that SCBC and TCC have common origins, establish DNA methylation of some tumor suppressors as frequent occurrences in both histopathologies, and suggest that MGMT methylation may be an SCBC-specific epimutation.]. 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:18192966
;
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:NP307332.RAbnTzQBtF3DLV04FIlKBO3I34awN7H5xxVaknZQB6Hsk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}