@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E
> .
@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:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_head
{
this:
np:hasAssertion
dgn-np:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_assertion
;
np:hasProvenance
dgn-np:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_provenance
;
np:hasPublicationInfo
dgn-np:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_assertion
a
np:Assertion
.
dgn-np:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_provenance
a
np:Provenance
.
dgn-np:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_assertion
{
miriam-gene:57104
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN6d3e3bc12a1f37534f43e587542a6d29
sio:SIO_000628
miriam-gene:57104
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_provenance
{
dgn-np:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_assertion
dcterms:description
"[A subgroup of neutral lipid storage disease has been recently associated with myopathy (NLSDM) and attributed to mutations in the gene (PNPLA2) encoding an adipose triglyceride lipase involved in the degradation of intracellular triglycerides.]. 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:18952067
;
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:NP265521.RAaBe0vgXiv5dTgEkYdareqDx71Eyin8xs1nsIYCcXc_E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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" .
}