@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0
> .
@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:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_head
{
this:
np:hasAssertion
dgn-np:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_assertion
;
np:hasProvenance
dgn-np:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_provenance
;
np:hasPublicationInfo
dgn-np:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_assertion
a
np:Assertion
.
dgn-np:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_provenance
a
np:Provenance
.
dgn-np:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_assertion
{
miriam-gene:2309
a
ncit:C16612
.
lld:C0232939
a
ncit:C7057
.
dgn-gda:DGN0c9604b1c8a6273723a8cadd42446227
sio:SIO_000628
miriam-gene:2309
,
lld:C0232939
;
a
sio:SIO_001121
.
}
dgn-np:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_provenance
{
dgn-np:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_assertion
dcterms:description
"[Then, to determine if heterozygous or homozygous polymorphisms or mutations of the human orthologue FOXO3 contribute to POF or idiopathic primary amenorrhea (PA), we sequenced the exons and flanking splice sequences of the gene in a large number of women with idiopathic POF (n = 273) or PA (n = 29).]. 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:17959613
;
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:NP777630.RAe4a310PkM9bRwnz9yFR_RQrxs1l2VQSa9SXPgUjQ9W0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}