@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448
> .
@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:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_head
{
this:
np:hasAssertion
dgn-np:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_assertion
;
np:hasProvenance
dgn-np:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_provenance
;
np:hasPublicationInfo
dgn-np:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_assertion
a
np:Assertion
.
dgn-np:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_provenance
a
np:Provenance
.
dgn-np:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_assertion
{
miriam-gene:8288
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGNd02e18fdabad24183aa7b97a0079c13d
sio:SIO_000628
miriam-gene:8288
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_provenance
{
dgn-np:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_assertion
dcterms:description
"[Our data indicate that the Arg200Trp substitution impairs the interaction of VHL with HIF1alpha, reducing the rate of degradation of HIF1alpha and resulting in increased expression of downstream target genes including EPO (encoding erythropoietin), SLC2A1 (also known as GLUT1, encoding solute carrier family 2 (facilitated glucose transporter), member 1), TF (encoding transferrin), TFRC (encoding transferrin receptor (p90, CD71)) and VEGF (encoding vascular endothelial growth factor).]. 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:12415268
;
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:NP649838.RAl2BzpH5H6r9kPOnBB0hX77t8hMI0yx9S7cwGM_xO448130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:31+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" .
}