@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c
> .
@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:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_head
{
this:
np:hasAssertion
dgn-np:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_assertion
;
np:hasProvenance
dgn-np:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_provenance
;
np:hasPublicationInfo
dgn-np:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_assertion
a
np:Assertion
.
dgn-np:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_provenance
a
np:Provenance
.
dgn-np:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_assertion
{
miriam-gene:3283
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNe431c911ad03d58e15be99e5b7ab51a3
sio:SIO_000628
miriam-gene:3283
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_provenance
{
dgn-np:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_assertion
dcterms:description
"[A total of 275 EH patients and 286 controls were genotyped for four SNPs of the HSD3B1 gene (rs3765945, rs3088283, rs6203, and rs1047303) and for two SNPs of the HSD3B2 gene (rs2854964 and rs1819698).]. 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:20660004
;
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:NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6_iomRmdanVo22c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}