@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI
> .
@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/v3.0.0/void/
> .
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_head
{
this:
np:hasAssertion
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_assertion
;
np:hasProvenance
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_provenance
;
np:hasPublicationInfo
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_assertion
a
np:Assertion
.
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_provenance
a
np:Provenance
.
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_assertion
{
miriam-gene:3014
a
ncit:C16612
.
lld:C0004509
a
ncit:C7057
.
dgn-gda:DGN5fff760ee516576bf1ed33d13612eced
sio:SIO_000628
miriam-gene:3014
,
lld:C0004509
;
a
sio:SIO_001122
.
}
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_provenance
{
dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_assertion
dcterms:description
"[To investigate the possible association of variations of the H2AX gene with spermatogenic impairment in humans, mutation screening of the entire coding region of this gene was carried out in 302 patients with azoospermia or severe oligospermia along with 198 normospermic controls.]. 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:18536151
;
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:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:38+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}