@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0
> .
@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:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_head
{
this:
np:hasAssertion
dgn-np:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_assertion
;
np:hasProvenance
dgn-np:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_provenance
;
np:hasPublicationInfo
dgn-np:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_assertion
a
np:Assertion
.
dgn-np:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_provenance
a
np:Provenance
.
dgn-np:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_assertion
{
miriam-gene:10566
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN4d8eeb84cba9f73f22f83d237fa4b04b
sio:SIO_000628
miriam-gene:10566
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_provenance
{
dgn-np:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_assertion
dcterms:description
"[We report the case of an infertile man with normal sperm count and total sperm immotility in which dysplasia of the fibrous sheath, Akap3, Akap4 gene deletions, meiotic segregation of chromosomes 18, X and Y and Y microdeletions were investigated.]. 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:15980003
;
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:NP798634.RAAzyhOogAy-lhYPWbO4DbbDBr05lSdVEFMPXZzym99U0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}