@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs
> .
@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:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_head
{
this:
np:hasAssertion
dgn-np:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_assertion
;
np:hasProvenance
dgn-np:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_provenance
;
np:hasPublicationInfo
dgn-np:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_assertion
a
np:Assertion
.
dgn-np:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_provenance
a
np:Provenance
.
dgn-np:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C2931838
a
ncit:C7057
.
dgn-gda:DGNc6111cd451c125648af36d694dd12770
sio:SIO_000628
miriam-gene:3630
,
lld:C2931838
;
a
sio:SIO_001121
.
}
dgn-np:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_provenance
{
dgn-np:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_assertion
dcterms:description
"[Much to our surprise, the genotype differences in BMI and insulin sensitivity in the whole population were attributable entirely to differences in the subgroup without FHD, whereas in the subgroup with FHD, the G allele had absolutely no effect.]. 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:11756320
;
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:NP857733.RAlfKuLQraMDXYjxkBlUZ8m-X-PKKWTFxhEmEUP7pjzfs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:44+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" .
}