@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA
> .
@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:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_head
{
this:
np:hasAssertion
dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_assertion
;
np:hasProvenance
dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_provenance
;
np:hasPublicationInfo
dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_assertion
a
np:Assertion
.
dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_provenance
a
np:Provenance
.
dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_assertion
{
miriam-gene:83983
a
ncit:C16612
.
lld:C0004509
a
ncit:C7057
.
dgn-gda:DGN99596a657494bfbebad785032523ef5c
sio:SIO_000628
miriam-gene:83983
,
lld:C0004509
;
a
sio:SIO_001121
.
}
dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_provenance
{
dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_assertion
dcterms:description
"[In order to investigate the possible relationships between variations, including mutations and polymorphisms of the TSSK4 gene and impaired spermatogenesis in humans, mutation screening of this gene in 372 patients with azoospermia or severe oligospermia and 220 controls was performed.]. 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:18390560
;
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:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}