@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw
> .
@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:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_head
{
this:
np:hasAssertion
dgn-np:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_assertion
;
np:hasProvenance
dgn-np:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_provenance
;
np:hasPublicationInfo
dgn-np:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_assertion
a
np:Assertion
.
dgn-np:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_provenance
a
np:Provenance
.
dgn-np:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_assertion
{
miriam-gene:5445
a
ncit:C16612
.
lld:C0020445
a
ncit:C7057
.
dgn-gda:DGN261b9a6f6bb7cb821779a735700e1988
sio:SIO_000628
miriam-gene:5445
,
lld:C0020445
;
a
sio:SIO_001121
.
}
dgn-np:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_provenance
{
dgn-np:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_assertion
dcterms:description
"[In our study we assessed the frequency and genotype distribution of the PON1 and PON2 polymorphisms in 197 patients with familial hypercholesterolemia (FH), to determine the possible association between these mutations and susceptibility for CVD.]. 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:11257265
;
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:NP225312.RAa67aeq0SCDfVY6Wfy4o9_UEdop7AnaRdQUHO1g5uevw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}