@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg
> .
@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:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_head
{
this:
np:hasAssertion
dgn-np:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_assertion
;
np:hasProvenance
dgn-np:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_provenance
;
np:hasPublicationInfo
dgn-np:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_assertion
a
np:Assertion
.
dgn-np:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_provenance
a
np:Provenance
.
dgn-np:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_assertion
{
miriam-gene:590
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNc684176d7269591416a5a226ea971ad3
sio:SIO_000628
miriam-gene:590
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_provenance
{
dgn-np:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_assertion
dcterms:description
"[data suggest that the BCHE-K allele increases the risk of coronary artery disease in the population (with and without DM) in western parts of Iran, and its presence intensifies the risk of coronary artery disease in type 2 diabetics ]. 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:17852836
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP134193.RAMZZ2Wfdk20KMgZ7USW1RrDmLyRwPZhc3mhjYKTrnAIg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:10+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" .
}