@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4
> .
@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 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:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_head
{
this:
np:hasAssertion
dgn-np:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_assertion
;
np:hasProvenance
dgn-np:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_provenance
;
np:hasPublicationInfo
dgn-np:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_assertion
a
np:Assertion
.
dgn-np:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_provenance
a
np:Provenance
.
dgn-np:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_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:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_provenance
{
dgn-np:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_assertion
dct: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 whether an association of K-IV-2 repeat length with CHD exists or not.]. 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-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}