@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_head
{
this:
np:hasAssertion
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_assertion
;
np:hasProvenance
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_provenance
;
np:hasPublicationInfo
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_assertion
a
np:Assertion
.
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_provenance
a
np:Provenance
.
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGNe431f1a007d2dab3823a32752075ffd9
sio:SIO_000628
miriam-gene:183
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_provenance
{
dgn-np:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_assertion
dcterms:description
"[The association of the angiotensinogen (AGT) gene variation at codon 235, the T235 variant, with hypertension induced by erythropoietin (Epo) was investigated in patients with progressive renal disease requiring treatment for renal anemia with Epo.]. 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:11675943
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP334123.RAjnT1elOkEw4UMn0-l52NjDXXrKBWZp3GymTwoaK7m_0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:17+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}