@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_assertion
;
np:hasProvenance
dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_provenance
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np:hasPublicationInfo
dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_assertion
a
np:Assertion
.
dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_provenance
a
np:Provenance
.
dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_assertion
{
miriam-gene:23626
a
ncit:C16612
.
lld:C0085215
a
ncit:C7057
.
dgn-gda:DGNb0a61e372e7ca280793e46534737bb99
sio:SIO_000628
miriam-gene:23626
,
lld:C0085215
;
a
sio:SIO_001122
.
}
dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_provenance
{
dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_assertion
dcterms:description
"[The goal of this study was to determine whether mutations of meiotic genes, such as disrupted meiotic cDNA (DMC1), MutS homolog (MSH4), MSH5, and S. cerevisiae homolog (SPO11), were associated with premature ovarian failure (POF).]. 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:18166824
;
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:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:46+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" .
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