@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM
> .
@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:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_head
{
this:
np:hasAssertion
dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_assertion
;
np:hasProvenance
dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_provenance
;
np:hasPublicationInfo
dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_assertion
a
np:Assertion
.
dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_provenance
a
np:Provenance
.
dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_assertion
{
miriam-gene:50511
a
ncit:C16612
.
lld:C1847540
a
ncit:C7057
.
dgn-gda:DGN799ea9cd691c8bb3014ff046523d4942
sio:SIO_000628
miriam-gene:50511
,
lld:C1847540
;
a
sio:SIO_001121
.
}
dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_provenance
{
dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_assertion
dcterms:description
"[On the basis of the results, we agree with the idea that SYCP3 mutations are not associated with the genetic susceptibility for meiotic arrest in infertile male patients with nonobstructive azoospermia in the Turkish population and that further studies investigating the other components of the synaptonemal complex protein (SYCP1, SYCP2) should be conducted.]. 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:22670862
;
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:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:18+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" .
}