@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ
> .
@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:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_head
{
this:
np:hasAssertion
dgn-np:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_assertion
;
np:hasProvenance
dgn-np:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_assertion
a
np:Assertion
.
dgn-np:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_provenance
a
np:Provenance
.
dgn-np:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_assertion
{
miriam-gene:8653
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGNf6551f895fe86d86d59e44b374c9fc8c
sio:SIO_000628
miriam-gene:8653
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_provenance
{
dgn-np:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_assertion
dcterms:description
"[Partial AZF deletions including single AZF Y genes can cause the same testicular pathology as the corresponding complete deletion (e.g., DDX3Y gene deletions in AZFa), or might not be associated with male infertility at all (e.g., some BPY2, CDY1, DAZ gene deletions in AZFc).]. 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:22992914
;
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:NP438301.RAPZ9Cblc03fF0RQ986vZ1j-V-3bOQp0E_rh13PbjoQXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}