@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY
> .
@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:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_head
{
this:
np:hasAssertion
dgn-np:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_assertion
;
np:hasProvenance
dgn-np:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_provenance
;
np:hasPublicationInfo
dgn-np:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_assertion
a
np:Assertion
.
dgn-np:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_provenance
a
np:Provenance
.
dgn-np:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_assertion
{
miriam-gene:2819
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN2ccef6e71a86a670fd3ba4bcbbddfe53
sio:SIO_000628
miriam-gene:2819
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_provenance
{
dgn-np:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_assertion
dcterms:description
"[Functional consequences of the mutation were evaluated by measuring intracellular concentrations of cholesterol and triglyceride as well as triglyceride secretion in HepG2 (hepatocellular carcinoma) human cells lines overexpressing normal and mutant GPD1 cDNA.]. 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:22226083
;
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:NP881217.RAm_DcpiHCDf1Hw15XHlr8qgHSpOJaOxDSI4sq5zfQLaY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}