@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI
> .
@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:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_head
{
this:
np:hasAssertion
dgn-np:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_assertion
;
np:hasProvenance
dgn-np:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_provenance
;
np:hasPublicationInfo
dgn-np:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_assertion
a
np:Assertion
.
dgn-np:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_provenance
a
np:Provenance
.
dgn-np:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_assertion
{
miriam-gene:23617
a
ncit:C16612
.
lld:C0004509
a
ncit:C7057
.
dgn-gda:DGN48560cc0d834c8bac59183ae85fa077d
sio:SIO_000628
miriam-gene:23617
,
lld:C0004509
;
a
sio:SIO_001121
.
}
dgn-np:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_provenance
{
dgn-np:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_assertion
dcterms:description
"[To explore the possible association between mutations in the TSSK2 gene and idiopathic infertility in humans, mutation screening of the gene in 494 patients with azoospermia or severe oligozoospermia and 357 fertile controls was performed using denaturing high-performance liquid chromatography and DNA sequencing.]. 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:19926886
;
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:NP788092.RAg9ixQ8e_hokmChJYEtulDuxSClxIQPiLw5K-Tt89bcI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}