@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_head
{
this:
np:hasAssertion
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_assertion
;
np:hasProvenance
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_provenance
;
np:hasPublicationInfo
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_assertion
a
np:Assertion
.
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_provenance
a
np:Provenance
.
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_assertion
{
miriam-gene:1617
a
ncit:C16612
.
lld:C0028960
a
ncit:C7057
.
dgn-gda:DGNced5911d48280b36224b9f0b88e93f7f
sio:SIO_000628
miriam-gene:1617
,
lld:C0028960
;
a
sio:SIO_001122
.
}
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_provenance
{
dgn-np:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_assertion
dcterms:description
"[The frequency of partial copy deletion of DAZ gene in Chinese idiopathic azoospermia or severe oligozoospermia patients is much higher than that of fertile controls, suggesting that the deletion of DAZ1/DAZ2 may be one of the important genetic etiological factors of spermatogenesis damage.]. 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:15476166
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP88407.RA0YZ2vYA6skMUdkYGf5yuSNig2cf5UjS_3oI-6a6i9CY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:28+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}