@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA
> .
@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:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_head
{
this:
np:hasAssertion
dgn-np:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_assertion
;
np:hasProvenance
dgn-np:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_provenance
;
np:hasPublicationInfo
dgn-np:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_assertion
a
np:Assertion
.
dgn-np:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_provenance
a
np:Provenance
.
dgn-np:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_assertion
{
miriam-gene:668
a
ncit:C16612
.
lld:C1401084
a
ncit:C7057
.
dgn-gda:DGNdaa2016a2f461b2b99a6827d57547593
sio:SIO_000628
miriam-gene:668
,
lld:C1401084
;
a
sio:SIO_001121
.
}
dgn-np:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_provenance
{
dgn-np:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_assertion
dcterms:description
"[This report shows the importance of family history and genetic analysis in the evaluation of patients with POF and corroborates the relationship between mutations on the FOXL2 gene and ovarian insufficiency.]. 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:19969293
;
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:NP493520.RAexgCahzhtHRgjPaLPDUSnVNoR4ox9qhmCFbPxYpHPgA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}