@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8
> .
@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:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_head
{
this:
np:hasAssertion
dgn-np:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_assertion
;
np:hasProvenance
dgn-np:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_provenance
;
np:hasPublicationInfo
dgn-np:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_assertion
a
np:Assertion
.
dgn-np:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_provenance
a
np:Provenance
.
dgn-np:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_assertion
{
miriam-gene:8431
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGNdc65e0d1bb3cfa1ea3292efbcc7a1666
sio:SIO_000628
miriam-gene:8431
,
lld:C0025517
;
a
sio:SIO_001121
.
}
dgn-np:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_provenance
{
dgn-np:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_assertion
dcterms:description
"[The fact that SHP controls a complex set of genes in multiple metabolic pathways suggests the intriguing possibility of developing new therapeutics for metabolic diseases, including fatty liver, dyslipidemia and obesity, by regulating SHP with small molecules.]. 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:20970497
;
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:NP192970.RALp2G7FI4BSxVtQnwxAJl5He_PCamSupJXxiJAmdnkH8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:46+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" .
}