@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4
> .
@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:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_head
{
this:
np:hasAssertion
dgn-np:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_assertion
;
np:hasProvenance
dgn-np:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_provenance
;
np:hasPublicationInfo
dgn-np:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_assertion
a
np:Assertion
.
dgn-np:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_provenance
a
np:Provenance
.
dgn-np:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_assertion
{
miriam-gene:1655
a
ncit:C16612
.
lld:C0919267
a
ncit:C7057
.
dgn-gda:DGN59141d91061514cbcaf227423da19d70
sio:SIO_000628
miriam-gene:1655
,
lld:C0919267
;
a
sio:SIO_001121
.
}
dgn-np:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_provenance
{
dgn-np:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_assertion
dcterms:description
"[Real-time RT-PCR analysis showed that mRNA for HER2/neu and 3 SEREX-defined antigens, TOP2A, HOXB6 and DDX5, was more abundant in ovarian tumors than most normal tissues, including normal and benign ovarian tissues, suggesting that elevated expression of genes encoded within this region of chromosome 17 is a common event in ovarian tumors.]. 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:12532422
;
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:NP939549.RAkuVEVM-CAtl-40nUGt6s5gf7S42LAZ5mvh-fLefnvX4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}