@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU
> .
@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:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_head
{
this:
np:hasAssertion
dgn-np:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_assertion
;
np:hasProvenance
dgn-np:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_provenance
;
np:hasPublicationInfo
dgn-np:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_assertion
a
np:Assertion
.
dgn-np:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_provenance
a
np:Provenance
.
dgn-np:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_assertion
{
miriam-gene:2167
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN0bd60bb6f43bf4f625aeab041ee8c659
sio:SIO_000628
miriam-gene:2167
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_provenance
{
dgn-np:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_assertion
dcterms:description
"[The frequency of rs1054135 allelic variant was increased in OB, and was associated with increased FABP4 levels, while the presence of rs16909233 variant allele, although similar in OB and NOB, was associated with increased HOMA values.]. 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:20156355
;
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:NP349423.RAjGVq8VG3t4BmuuUbWRAku02XJL2KZvTUGMdCrGNBFLU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:25+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" .
}