@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI
> .
@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:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_head
{
this:
np:hasAssertion
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_assertion
;
np:hasProvenance
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_assertion
a
np:Assertion
.
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_provenance
a
np:Provenance
.
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_assertion
{
miriam-gene:270
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN25c9f19f4af2a1e75962f88bf70ac91b
sio:SIO_000628
miriam-gene:270
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_provenance
{
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_assertion
dcterms:description
"[In conclusion, there were no differences between the mutant AMPD1 allele carriers and CC homozygotes regarding surrogate values for atherosclerosis, endothelial function, dimensions and ejection fraction of the heart, glucose tolerance and other well-known cardiovascular risk factors, whereas plasminogen activator inhibitor-1 activity and von Willebrand levels were lower in the mutant AMPD1 allele carriers.]. 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:17565237
;
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:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}