@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA
> .
@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:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_head
{
this:
np:hasAssertion
dgn-np:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_assertion
;
np:hasProvenance
dgn-np:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_provenance
;
np:hasPublicationInfo
dgn-np:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_assertion
a
np:Assertion
.
dgn-np:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_provenance
a
np:Provenance
.
dgn-np:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_assertion
{
miriam-gene:4512
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGNf5f0dfa6a32065b9e71999c1ce545116
sio:SIO_000628
miriam-gene:4512
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_provenance
{
dgn-np:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_assertion
dcterms:description
"[Earlier we found the same for cytochrome c oxidase subunit I (COXI) Serial Analysis of Gene Expression (SAGE) showed lower content of the tags for all mitochondrial genes in GB SAGE libraries and together with our experimental data could serve as evidence of general inactivation of the mitochondrial genome in glioblastoma--the most malignant and abundant form of human brain tumor.]. 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:15639345
;
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:NP736338.RAXsS9F2awwiGWzE9Rw9nCNFLZhMCdkpGTaFvSC61bgtA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:27+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" .
}