@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_assertion
a
np:Assertion
.
dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_provenance
a
np:Provenance
.
dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_assertion
{
miriam-gene:337
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGNefcb27b17f264b0c7f8505301f307f6c
sio:SIO_000628
miriam-gene:337
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_provenance
{
dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_assertion
dcterms:description
"[Together with previous studies our results indicate that the relation between apo(a) genotypes, Lp(a) levels, and CHD may be heterogeneous across ethnic groups and that it depends on the genetic architecture of the Lp(a) trait in a given population whethe]. 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:12860258
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:24+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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
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"v4.0.0" .
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