@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ
> .
@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:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_head
{
this:
np:hasAssertion
dgn-np:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_assertion
;
np:hasProvenance
dgn-np:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_assertion
a
np:Assertion
.
dgn-np:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_provenance
a
np:Provenance
.
dgn-np:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_assertion
{
miriam-gene:875
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGNb09fcc141956e295c4c220905b5e0c08
sio:SIO_000628
miriam-gene:875
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_provenance
{
dgn-np:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_assertion
dcterms:description
"[In order to clarify whether cystathionine beta-synthase (CBS) could differentiate groups of patients with various vascular diagnosis, CBS was studied in cultured human skin fibroblasts from 99 human subjects diagnosed as homozygotes or heterozygotes for CBS deficiency or suffering from atherosclerotic vascular disease or Down's syndrome (prone to less atherosclerosis).]. 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:1385957
;
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:NP694573.RA3JCdGLKNdV4Kdrx-O3te5lgsJeu4wNx1Axc-Axz7fJQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:02+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" .
}