@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk
> .
@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:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_head
{
this:
np:hasAssertion
dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_assertion
;
np:hasProvenance
dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_provenance
;
np:hasPublicationInfo
dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_assertion
a
np:Assertion
.
dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_provenance
a
np:Provenance
.
dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C2673196
a
ncit:C7057
.
dgn-gda:DGN8abd94af49a97730abcee6100fa3e01e
sio:SIO_000628
miriam-gene:348
,
lld:C2673196
;
a
sio:SIO_001122
.
}
dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_provenance
{
dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_assertion
dcterms:description
"[ Apo E1 (Gln 156-Gly 173-->0) is a novel mutation of apo E that may be etiologically related to LPG and to the development of atherosclerosis. The result of this family study suggests that the occurrence of LPG may involve other genetic or environmental factors.]. 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:10504484
;
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:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}