@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo
> .
@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:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_head
{
this:
np:hasAssertion
dgn-np:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_assertion
;
np:hasProvenance
dgn-np:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_provenance
;
np:hasPublicationInfo
dgn-np:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_assertion
a
np:Assertion
.
dgn-np:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_provenance
a
np:Provenance
.
dgn-np:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_assertion
{
miriam-gene:341
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN90f788ebae97ed7da78900e46eadb813
sio:SIO_000628
miriam-gene:341
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_provenance
{
dgn-np:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_assertion
dcterms:description
"[Obese obob mice with strong overexpression of the human apolipoprotein C1 (APOC1) exhibit excessive free fatty acid (FFA) and triglyceride (TG) levels and severely reduced body weight (due to the absence of subcutaneous adipose tissue) and skin abnormalities.]. 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:14523051
;
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:NP618672.RAVmrf5V9E21Crt3iSQI1FVhBU9ZrMlZbNYWlk_OUxgJo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:14+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" .
}