@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM
> .
@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:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_head
{
this:
np:hasAssertion
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_assertion
;
np:hasProvenance
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_provenance
;
np:hasPublicationInfo
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_assertion
a
np:Assertion
.
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_provenance
a
np:Provenance
.
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_assertion
{
miriam-gene:4049
a
ncit:C16612
.
lld:C0020459
a
ncit:C7057
.
dgn-gda:DGN5f928bd0828cea5c52c0eb99dd2d56b3
sio:SIO_000628
miriam-gene:4049
,
lld:C0020459
;
a
sio:SIO_001121
.
}
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_provenance
{
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_assertion
dcterms:description
"[Homozygosity for rare alleles of the LTA 252A>G polymorphisms was associated with features of metabolic syndrome such as hyperinsulinemia, dyslipidemia, small LDL particle and low adiponectin level in CAD patients, suggesting that CAD patients with LTA 252GG are at high risk and needed an intensive intervention against further progression.]. 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:17640627
;
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:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}