@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_head
{
this:
np:hasAssertion
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_assertion
;
np:hasProvenance
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_provenance
;
np:hasPublicationInfo
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_assertion
a
np:Assertion
.
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_provenance
a
np:Provenance
.
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_assertion
{
miriam-gene:723961
a
ncit:C16612
.
lld:C0206081
a
ncit:C7057
.
dgn-gda:DGN30b62247bae666a4d4a903377a57b931
sio:SIO_000628
miriam-gene:723961
,
lld:C0206081
;
a
sio:SIO_001121
.
}
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_provenance
{
dgn-np:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_assertion
dcterms:description
"[Genetic lipodystrophic syndromes are rare diseases characterized by generalized or partial fat atrophy (lipoatrophy) associated with severe metabolic complications such as insulin resistance (IR), diabetes, dyslipidemia, nonalcoholic fatty liver disease, and ovarian hyperandrogenism.]. 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:24026869
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP1007632.RAbhIn1jy84N13lzbpy0roQl4GRkqACuTRPNMh8R3j6PU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:48:04+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}