@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ
> .
@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:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_head
{
this:
np:hasAssertion
dgn-np:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_assertion
;
np:hasProvenance
dgn-np:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_assertion
a
np:Assertion
.
dgn-np:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_provenance
a
np:Provenance
.
dgn-np:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0334121
a
ncit:C7057
.
dgn-gda:DGNba3257ef72f628efe22c958a936b8d15
sio:SIO_000628
miriam-gene:1636
,
lld:C0334121
;
a
sio:SIO_001121
.
}
dgn-np:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_provenance
{
dgn-np:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_assertion
dcterms:description
"[Our findings confirm an increased prevalence of macrovascular disease in SSc patients and show that IMT is greater in patients carrying the ACE DD and ID genotype in comparison with II homozygotes.]. 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:17264090
;
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:NP389683.RArLg1p-0qIyzF2unUpnztaWf9qC7eFLQSwxscpViefkQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}