@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg
> .
@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:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_head
{
this:
np:hasAssertion
dgn-np:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_assertion
;
np:hasProvenance
dgn-np:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_provenance
;
np:hasPublicationInfo
dgn-np:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_assertion
a
np:Assertion
.
dgn-np:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_provenance
a
np:Provenance
.
dgn-np:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0023787
a
ncit:C7057
.
dgn-gda:DGNac8f3174aa166a8a739010916503ff71
sio:SIO_000628
miriam-gene:3630
,
lld:C0023787
;
a
sio:SIO_001121
.
}
dgn-np:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_provenance
{
dgn-np:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_assertion
dcterms:description
"[Genetic lipodystrophies are rare disorders characterized by partial or complete loss of adipose tissue and predisposition to insulin resistance and its complications such as diabetes mellitus, hypertriglyceridemia, hepatic steatosis, acanthosis nigricans, and polycystic ovarian syndrome.]. 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:20534754
;
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:NP268997.RAvBeeZFJbAoM3-QHw_N5_K8HY1I1agSKuZ8th6c7GmCg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}