@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c
> .
@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:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_head
{
this:
np:hasAssertion
dgn-np:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_assertion
;
np:hasProvenance
dgn-np:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_provenance
;
np:hasPublicationInfo
dgn-np:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_assertion
a
np:Assertion
.
dgn-np:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_provenance
a
np:Provenance
.
dgn-np:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C1261287
a
ncit:C7057
.
dgn-gda:DGN9cc6d2b252fc86cceddd2537c1bdac7c
sio:SIO_000628
miriam-gene:5444
,
lld:C1261287
;
a
sio:SIO_001121
.
}
dgn-np:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_provenance
{
dgn-np:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_assertion
dcterms:description
"[The haplotypes of the G(-907)C, A(-162)G and C(-107)T polymorphisms within the 5' region of the PON1 gene were determined in 99 patients and 66 controls who were evaluated angiographically for the presence and extent of stenosis in coronary arteries.]. 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:18433845
;
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:NP488864.RA3a88uKZ6S23i6ElIzUN7TuR1lndPOVJMWK80vip92_c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}