@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg
> .
@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:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_head
{
this:
np:hasAssertion
dgn-np:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_assertion
;
np:hasProvenance
dgn-np:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_provenance
;
np:hasPublicationInfo
dgn-np:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_assertion
a
np:Assertion
.
dgn-np:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_provenance
a
np:Provenance
.
dgn-np:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_assertion
{
miriam-gene:6755
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN8fd04e5719198af18f6655b4041df2f0
sio:SIO_000628
miriam-gene:6755
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_provenance
{
dgn-np:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_assertion
dcterms: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: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:NP893272.RADcfp4N5njnynfFUVrB2yB5z9MR8W_Jdl7vv9rxPSqfg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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" .
}