@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo
> .
@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:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_head
{
this:
np:hasAssertion
dgn-np:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_assertion
;
np:hasProvenance
dgn-np:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_provenance
;
np:hasPublicationInfo
dgn-np:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_assertion
a
np:Assertion
.
dgn-np:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_provenance
a
np:Provenance
.
dgn-np:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_assertion
{
miriam-gene:668
a
ncit:C16612
.
lld:C0025322
a
ncit:C7057
.
dgn-gda:DGN4aa17c0e6d3db52e5aa715743639fac7
sio:SIO_000628
miriam-gene:668
,
lld:C0025322
;
a
sio:SIO_001121
.
}
dgn-np:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_provenance
{
dgn-np:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_assertion
dcterms:description
"[The results came back with no novel mutations but one common 30 bp duplication within FOXL2 polyalanine tract in the abovementioned POF plus BPES patient, suggesting mutations in FOXL2 gene was not common among Chinese patients with 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:20222838
;
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:NP243867.RA_By3RIS4ElP2ehoSMYBSPjRc5PQybdZ6lb6eXIqvryo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}