@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk
> .
@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:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_head
{
this:
np:hasAssertion
dgn-np:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_assertion
;
np:hasProvenance
dgn-np:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_provenance
;
np:hasPublicationInfo
dgn-np:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_assertion
a
np:Assertion
.
dgn-np:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_provenance
a
np:Provenance
.
dgn-np:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_assertion
{
miriam-gene:132
a
ncit:C16612
.
lld:C0024314
a
ncit:C7057
.
dgn-gda:DGNfe6e677295f030d8dd2be6df9a4ed6bd
sio:SIO_000628
miriam-gene:132
,
lld:C0024314
;
a
sio:SIO_001121
.
}
dgn-np:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_provenance
{
dgn-np:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_assertion
dcterms:description
"[They may be used to mimic the genetic deficiency of the enzyme, in lymphoproliferative disorders or immunosuppressive therapy (i.e., in graft rejection), to potentiate the effect of antileukemic or antiviral nucleosides, and, together with adenosine kinase, to reduce breakdown of adenosine in inflammation, hypertension, and ischemic injury.]. 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:11223861
;
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:NP440208.RAMZI8upx4vQA6T2jdiysP4oBYSo2Q9AAZtupUojWsiCk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}