@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_head
{
this:
np:hasAssertion
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_assertion
;
np:hasProvenance
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance
;
np:hasPublicationInfo
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_assertion
a
np:Assertion
.
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance
a
np:Provenance
.
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_assertion
{
miriam-gene:668
a
ncit:C16612
.
lld:C1862260
a
ncit:C7057
.
dgn-gda:DGN608f9d5c89972ecff59baa9e8ad29028
sio:SIO_000628
miriam-gene:668
,
lld:C1862260
;
a
sio:SIO_001121
.
}
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance
{
dgn-np:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_assertion
dcterms:description
"[MDR analysis for intragenic mutations of FOXL2 gene reported in previous BPES studies indicated that the mutations which led to much stronger disturbance of amino acid sequence were responsible for more type I BPES, while other kinds of mutation were responsible for more type II BPES.]. 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:19592504
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:25+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}