@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8
> .
@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:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_head
{
this:
np:hasAssertion
dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_assertion
;
np:hasProvenance
dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_provenance
;
np:hasPublicationInfo
dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_assertion
a
np:Assertion
.
dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_provenance
a
np:Provenance
.
dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_assertion
{
miriam-gene:6696
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGN99187c7b9aa6dad5132293ea07b31d24
sio:SIO_000628
miriam-gene:6696
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_provenance
{
dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_assertion
dcterms:description
"[Among a panel of known hypoxia-inducible genes, OPN and CA9 emerge as most consistently induced by in vitro hypoxia in human GBM cell lines and most specifically expressed in patient GBM tumor tissue, rendering these two genes attractive targets for hypoxia-directed treatment approaches.]. 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:17524506
;
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:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:39+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" .
}