@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ
> .
@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:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_head
{
this:
np:hasAssertion
dgn-np:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_assertion
;
np:hasProvenance
dgn-np:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_assertion
a
np:Assertion
.
dgn-np:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_provenance
a
np:Provenance
.
dgn-np:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0154208
a
ncit:C7057
.
dgn-gda:DGN2e2ea41e90f23d12dcd9080e1ced7dff
sio:SIO_000628
miriam-gene:2332
,
lld:C0154208
;
a
sio:SIO_001121
.
}
dgn-np:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_provenance
{
dgn-np:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_assertion
dcterms:description
"[The results obtained strengthen the correlation between FMR1 expansion and POF and suggest that the manifestation of the ovarian dysfunction could be influenced both by the pattern of interruption of the CGG repeat and by X-inactivation.]. 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:16361284
;
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:NP305367.RATDtRa79FUzIw2-98doJFAEz4Sr6mzeXXrBG9nvZ0kXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}