@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c
> .
@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:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_head
{
this:
np:hasAssertion
dgn-np:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_assertion
;
np:hasProvenance
dgn-np:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_provenance
;
np:hasPublicationInfo
dgn-np:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_assertion
a
np:Assertion
.
dgn-np:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_provenance
a
np:Provenance
.
dgn-np:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_assertion
{
miriam-gene:8639
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN98ec8a5fea98868f69e6cf88e7897c7e
sio:SIO_000628
miriam-gene:8639
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_provenance
{
dgn-np:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_assertion
dcterms:description
"[It has been speculated that production of cytotoxic products of SSAO may cause endothelial damage and thus contribute to the development of diabetic vascular complications such as retino-, nephro-, and neuropathies as a result of SSAO activity.In order to explore the possibility that high SSAO activity contributes to the development of vascular complications in diabetes, we have performed two studies in patients with Type-2 diabetes quantifying plasma SSAO activity, HbA(1c), and urinary levels of the SSAO substrate, methylamine.]. 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:12686114
;
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:NP817451.RAkClf8G9o4Vut7yu6XpenhkHKc91CK_leRo0b1yWtk_c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:21+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" .
}