@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU
> .
@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 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:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_head
{
this:
np:hasAssertion
dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_assertion
;
np:hasProvenance
dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_provenance
;
np:hasPublicationInfo
dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_assertion
a
np:Assertion
.
dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_provenance
a
np:Provenance
.
dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_assertion
{
miriam-gene:875
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN8c1bdedec8198cbd4700109dc9236232
sio:SIO_000628
miriam-gene:875
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_provenance
{
dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_assertion
dc: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:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:36+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}