@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8
> .
@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:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_head
{
this:
np:hasAssertion
dgn-np:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_assertion
;
np:hasProvenance
dgn-np:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_provenance
;
np:hasPublicationInfo
dgn-np:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_assertion
a
np:Assertion
.
dgn-np:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_provenance
a
np:Provenance
.
dgn-np:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_assertion
{
miriam-gene:114548
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN9677864e0a526c45e8ecaec108d5325b
sio:SIO_000628
miriam-gene:114548
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_provenance
{
dgn-np:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_assertion
dcterms:description
"[Our results suggest that these two variants located in the coding region of the Apo AII gene are unlikely to contribute significantly to the level of plasma lipid variables and the risk of coronary heart disease (CHD) in the European population.]. 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:9001797
;
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:NP307850.RA7tjQ4YckMcuApS4eYUKZfO3ImkqLCYt0FmzjSS8nSo8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}