@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac
> .
@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:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_head
{
this:
np:hasAssertion
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_assertion
;
np:hasProvenance
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_provenance
;
np:hasPublicationInfo
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_assertion
a
np:Assertion
.
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_provenance
a
np:Provenance
.
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_assertion
{
miriam-gene:346673
a
ncit:C16612
.
lld:C0028960
a
ncit:C7057
.
dgn-gda:DGN08f5abdd435a93cf3d00dcc94b5a0d1d
sio:SIO_000628
miriam-gene:346673
,
lld:C0028960
;
a
sio:SIO_001121
.
}
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_provenance
{
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_assertion
dcterms:description
"[The genetic variant rs10269148 of STRA8 gene showed higher risk of spermatogenic impairment in the groups of abnormospermia (including azoospermia subgroup and oligozoospermia subgroup) and azoospermia than the controls with odds ratios and 95% confidence intervals of 2.52 (1.29-4.94) and 2.92 (1.41-6.06), respectively (Pā=ā0.006, 0.002 respective).]. 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:23320086
;
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:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:02+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" .
}