@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ
> .
@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:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_head
{
this:
np:hasAssertion
dgn-np:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_assertion
;
np:hasProvenance
dgn-np:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_assertion
a
np:Assertion
.
dgn-np:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_provenance
a
np:Provenance
.
dgn-np:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_assertion
{
miriam-gene:54583
a
ncit:C16612
.
lld:C0152264
a
ncit:C7057
.
dgn-gda:DGNcf26465fa8a1f2b553e99151d13dc0ad
sio:SIO_000628
miriam-gene:54583
,
lld:C0152264
;
a
sio:SIO_001121
.
}
dgn-np:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_provenance
{
dgn-np:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_assertion
dcterms:description
"[The variants display differential effects on catalytic rate and substrate binding, implying that partial inhibition or selective inhibition with regard to HIFalpha isoforms of PHD2 could result in the phenotype displayed by patients with familial erythrocytosis.]. 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:18834144
;
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:NP456749.RAoYPzUf5G5c4ImKurf0Iw99vaDb3DJtDntg7V2wsl5bQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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" .
}