@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc
> .
@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:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_head
{
this:
np:hasAssertion
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_assertion
;
np:hasProvenance
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_provenance
;
np:hasPublicationInfo
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_assertion
a
np:Assertion
.
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_provenance
a
np:Provenance
.
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_assertion
{
miriam-gene:412
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGNd9f5637636ff2dc1237508039589e083
sio:SIO_000628
miriam-gene:412
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_provenance
{
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_assertion
dcterms:description
"[To determine the prevalence of Y-chromosome microdeletions among infertile men and to correlate the clinical presentation of the men with specific deletions, microdeletion analysis in 53 infertile men (30 nonobstructive azoospermic, 23 severely oligozoospermic patients), and 100 age-matched, fathered normospermic men who had fathered children was performed by the multiplex PCR with 18 different Y-chromosome-specific STS primer sets, spanning the AZFa, AZFb, AZFd, and AZFc regions.]. 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:16084901
;
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:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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" .
}