@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng
> .
@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 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:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_head
{
this:
np:hasAssertion
dgn-np:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_assertion
;
np:hasProvenance
dgn-np:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_provenance
;
np:hasPublicationInfo
dgn-np:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_assertion
a
np:Assertion
.
dgn-np:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_provenance
a
np:Provenance
.
dgn-np:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_assertion
{
miriam-gene:356
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGN8fa52bc03a553eaa1fc6edee2376cd80
sio:SIO_000628
miriam-gene:356
,
lld:C0021364
;
a
sio:SIO_001122
.
}
dgn-np:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_provenance
{
dgn-np:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_assertion
dc:description
"[This study showed for the first time that functional variants of FAS and CASP8 might contribute to the dysfunctional apoptotic mechanism in germ cells, which could result in poor semen quality of ejaculated sperm.]. 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:19542541
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP80371.RATOzaH3sVCXQqI3YuhsLQGyTDKoA12kWA4qoo8W0Wzng130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}