@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM
> .
@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:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_head
{
this:
np:hasAssertion
dgn-np:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_assertion
;
np:hasProvenance
dgn-np:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_provenance
;
np:hasPublicationInfo
dgn-np:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_assertion
a
np:Assertion
.
dgn-np:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_provenance
a
np:Provenance
.
dgn-np:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGN43fe166c237abf218fb0037c3fad94a2
sio:SIO_000628
miriam-gene:3630
,
lld:C0025517
;
a
sio:SIO_001121
.
}
dgn-np:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_provenance
{
dgn-np:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_assertion
dcterms:description
"[The successful translation to clinical medicine of molecular genetic research on other rare monogenic metabolic disorders has stimulated the evaluation of such rare monogenic forms of insulin resistance as partial lipodystrophy resulting from mutations in either LMNA or PPARG genes.]. 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:15177263
;
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:NP252880.RAjBDAFXi_vInMx3U6cnBfjyRAYMmIv1sWx_O2uBPJrBM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:21+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" .
}