@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA
> .
@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:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_head
{
this:
np:hasAssertion
dgn-np:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_assertion
;
np:hasProvenance
dgn-np:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_provenance
;
np:hasPublicationInfo
dgn-np:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_assertion
a
np:Assertion
.
dgn-np:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_provenance
a
np:Provenance
.
dgn-np:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0085215
a
ncit:C7057
.
dgn-gda:DGN6a03446be6192446b4e2a03a5b0d33ed
sio:SIO_000628
miriam-gene:2332
,
lld:C0085215
;
a
sio:SIO_001122
.
}
dgn-np:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_provenance
{
dgn-np:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_assertion
dcterms:description
"[ Abnormal autoimmune function and expansions in triple CGG repeats on the FMR1 gene represent distinctively different etiologies for premature ovarian senescence in infertile patients and may, indeed, constitute its two principal causes.]. 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:18384784
;
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:NP43906.RARyd6RoFjXGZq8RZkarLF2HJ5IrvEvoIzSWtWXcZeTtA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}