@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s
> .
@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:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_head
{
this:
np:hasAssertion
dgn-np:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_assertion
;
np:hasProvenance
dgn-np:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_assertion
a
np:Assertion
.
dgn-np:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_provenance
a
np:Provenance
.
dgn-np:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_assertion
{
miriam-gene:83593
a
ncit:C16612
.
lld:C0004114
a
ncit:C7057
.
dgn-gda:DGN2371d159fa58f48f1254a423767a59ed
sio:SIO_000628
miriam-gene:83593
,
lld:C0004114
;
a
sio:SIO_001121
.
}
dgn-np:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_provenance
{
dgn-np:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_assertion
dcterms:description
"[RASSF1A (3p21.3), NORE1A (1q32.1) and BLU (3p21.3) have been shown to be downregulated by methylation in cancer, and PTEN (10q23.3) and MGMT (10q26.1) are located in areas commonly deleted in astrocytomas.]. 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:18616639
;
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:NP661072.RA0HSZbvrOnwwZgSa_BbMgx-UX4TNESvMAWtCaeS96c_s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}