@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw
> .
@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:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_head
{
this:
np:hasAssertion
dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_assertion
;
np:hasProvenance
dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_provenance
;
np:hasPublicationInfo
dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_assertion
a
np:Assertion
.
dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_provenance
a
np:Provenance
.
dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_assertion
{
miriam-gene:345
a
ncit:C16612
.
lld:C0242339
a
ncit:C7057
.
dgn-gda:DGN53ab6b8febd02033af63a0af786b06bb
sio:SIO_000628
miriam-gene:345
,
lld:C0242339
;
a
sio:SIO_001121
.
}
dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_provenance
{
dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_assertion
dcterms:description
"[The T-455C and C-482T APOC3 promoter region polymorphisms (SNPs) have recently been reported to predispose to dyslipidemia, insulin resistance, and nonalcoholic fatty liver disease (NAFLD) in Indian subjects, but the association with liver damage has not been evaluated so far.]. 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:21777557
;
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:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}