@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ
> .
@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 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:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_head
{
this:
np:hasAssertion
dgn-np:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_assertion
;
np:hasProvenance
dgn-np:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_assertion
a
np:Assertion
.
dgn-np:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_provenance
a
np:Provenance
.
dgn-np:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_assertion
{
miriam-gene:6754
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNf3dfecb859379c281757d69a84274ddd
sio:SIO_000628
miriam-gene:6754
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_provenance
{
dgn-np:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_assertion
dc:description
"[Our results suggest that genetic variation in the SSTR5 gene and, particularly, the rs4988483 single nucleotide polymorphism influence circulating IGFI and IGFBP3 hormone levels with no measurable effect on prostate cancer risk.]. 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:19423539
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP81190.RAVqAH2aw7NUzmpgfErjV0UCrkUSmKNdn8sk6qf4ZLPrQ130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:40+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}