@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM
> .
@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:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_head
{
this:
np:hasAssertion
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_assertion
;
np:hasProvenance
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_provenance
;
np:hasPublicationInfo
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_assertion
a
np:Assertion
.
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_provenance
a
np:Provenance
.
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_assertion
{
miriam-gene:717
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN56cd6a32d5616f1f8d55f60197790ca8
sio:SIO_000628
miriam-gene:717
,
lld:C0242383
;
a
sio:SIO_001122
.
}
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_provenance
{
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_assertion
dcterms:description
"[The HDL-raising allele of the LIPC gene (T) was associated with a reduced risk of AMD. Higher total cholesterol and LDL levels were associated with increased risk, whereas higher HDL levels tended to reduce the risk of AMD. The specific mechanisms underlying the association between AMD and LIPC require further investigation.]. 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:20888482
;
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:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}