@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE
> .
@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:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_head
{
this:
np:hasAssertion
dgn-np:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_assertion
;
np:hasProvenance
dgn-np:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_provenance
;
np:hasPublicationInfo
dgn-np:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_assertion
a
np:Assertion
.
dgn-np:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_provenance
a
np:Provenance
.
dgn-np:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_assertion
{
miriam-gene:11188
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNac26a462665897743f90545ca07f1c48
sio:SIO_000628
miriam-gene:11188
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_provenance
{
dgn-np:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_assertion
dcterms:description
"[These results are consistent with the expectation that intermediate measures of insulin resistance and visceral adiposity are heritable, and that the IRAS Family Study has statistical power to detect these intermediate phenotypes of type 2 diabetes and atherosclerosis.]. 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:12684185
;
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:NP459058.RAH2ThEm6eX28wMM6phtc2XIdpNVdKCTmquKcV8kvnCvE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:33+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" .
}