@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s
> .
@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:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_head
{
this:
np:hasAssertion
dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_assertion
;
np:hasProvenance
dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_provenance
;
np:hasPublicationInfo
dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_assertion
a
np:Assertion
.
dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_provenance
a
np:Provenance
.
dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNde1ae52af80b7b860bf349ac1a799ba7
sio:SIO_000628
miriam-gene:3949
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_provenance
{
dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_assertion
dcterms:description
"[An improved understanding of etiologically complex pathologies involving the interplay of genes and the environment, such as atherosclerosis and systemic hypertension, has led to the identification of new targets for gene therapy, with the potential to alleviate inherited genetic defects such as familial hypercholesterolemia.]. 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:11711525
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}