@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A
> .
@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:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_head
{
this:
np:hasAssertion
dgn-np:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_assertion
;
np:hasProvenance
dgn-np:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_provenance
;
np:hasPublicationInfo
dgn-np:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_assertion
a
np:Assertion
.
dgn-np:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_provenance
a
np:Provenance
.
dgn-np:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_assertion
{
miriam-gene:3643
a
ncit:C16612
.
lld:C0000889
a
ncit:C7057
.
dgn-gda:DGN58c7c59b7dd350c5f69aefdb08e67ae8
sio:SIO_000628
miriam-gene:3643
,
lld:C0000889
;
a
sio:SIO_001121
.
}
dgn-np:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_provenance
{
dgn-np:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_assertion
dcterms:description
"[Defects in the insulin receptor gene causing insulin resistance and AN are well recognized, but recent data in several other syndromes of this association, including lipodystrophic disorders, have identified causative defects in other pathways.]. 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:12452857
;
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:NP699182.RAM05Q3rVXnnwCK5Ddp-27hFen61lV7adYPcn9xcKMk_A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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" .
}