@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw
> .
@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:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_head
{
this:
np:hasAssertion
dgn-np:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion
;
np:hasProvenance
dgn-np:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_provenance
;
np:hasPublicationInfo
dgn-np:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion
a
np:Assertion
.
dgn-np:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_provenance
a
np:Provenance
.
dgn-np:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion
{
miriam-gene:1617
a
ncit:C16612
.
lld:C0004509
a
ncit:C7057
.
dgn-gda:DGN882e275b53a749b549ea29ef8c1fd0d6
sio:SIO_000628
miriam-gene:1617
,
lld:C0004509
;
a
sio:SIO_001122
.
}
dgn-np:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_provenance
{
dgn-np:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion
dcterms:description
"[There is a high frequency of chromosomal abnormality and DAZ gene copy deletion in patients with azoospermia and oligospermia, which suggests that chromosomal abnormality and partial and complete deletion of DAZ gene copy might be important genetic causes of Chinese male infertility.]. 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:16078663
;
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:NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:31+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" .
}