@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ
> .
@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:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_head
{
this:
np:hasAssertion
dgn-np:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_assertion
;
np:hasProvenance
dgn-np:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_assertion
a
np:Assertion
.
dgn-np:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_provenance
a
np:Provenance
.
dgn-np:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN63f67d11585da87492ee8e5f35457d95
sio:SIO_000628
miriam-gene:4000
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_provenance
{
dgn-np:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_assertion
dcterms:description
"[FPLD is further characterized by muscular hypertrophy, hyperandrogenism, acanthosis nigricans, hepatomegaly with steatosis and at the biological level, marked hypertriglyceridaemia, low HDL cholesterol, insulin resistance and altered glucose tolerance or diabetes.]. 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:15773753
;
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:NP357237.RA3qpOtYDfeE4lnhxl51V8ciORoH5yfIQm24rtAmQkMtQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:29+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" .
}