@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY
> .
@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/
> .
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_head
{
this:
np:hasAssertion
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_assertion
;
np:hasProvenance
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_assertion
a
np:Assertion
.
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_provenance
a
np:Provenance
.
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNc525c6970b6c9cb15be95433e11af137
sio:SIO_000628
miriam-gene:348
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_provenance
{
dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_assertion
dcterms:description
"[The apoE polymorphism affects the serum lipoprotein levels, and the ESRD patients who are e4 and e2 allele carriers are more likely to present an atherogenic lipoprotein profile that may be a major factor associated with increased risk of 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:25155022
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:56+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}