@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw
> .
@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:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_head
{
this:
np:hasAssertion
dgn-np:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_assertion
;
np:hasProvenance
dgn-np:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_provenance
;
np:hasPublicationInfo
dgn-np:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_assertion
a
np:Assertion
.
dgn-np:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_provenance
a
np:Provenance
.
dgn-np:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_assertion
{
miriam-gene:7391
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNf92b13cc290b18e6e666cdad6df94021
sio:SIO_000628
miriam-gene:7391
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_provenance
{
dgn-np:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_assertion
dcterms:description
"[The hepatic nuclear factor 4alpha (HNF4alpha) gene partly explains the linkage peak on chromosome 20, while the upstream transcription factor (USF1) is associated with familial combined hyperlipidaemia (FCHL) and maps close to the type 2 diabetes associated 1q peak.]. 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:16035391
;
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:NP195529.RARhzcTxygLKCT-DOLqbumUNpoWjX-Rs68QQZKcHYNzfw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}