@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY
> .
@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:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_head
{
this:
np:hasAssertion
dgn-np:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_assertion
;
np:hasProvenance
dgn-np:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_provenance
;
np:hasPublicationInfo
dgn-np:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_assertion
a
np:Assertion
.
dgn-np:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_provenance
a
np:Provenance
.
dgn-np:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_assertion
{
miriam-gene:2138
a
ncit:C16612
.
lld:C1861537
a
ncit:C7057
.
dgn-gda:DGN32f3ef868bd50b6c655e9d32422d31c0
sio:SIO_000628
miriam-gene:2138
,
lld:C1861537
;
a
sio:SIO_001121
.
}
dgn-np:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_provenance
{
dgn-np:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_assertion
dcterms:description
"[Recent characterization of one OFC patient shed some light on the controversy over whether OFC and BOR are the same disease, and led to the hypothesis that OFC is caused by contiguous deletions of EYA1 and adjacent genes.]. 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:16441263
;
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:NP829825.RAb6Ujjg5LoNVQ0Q8aqwnMvd07yJ69t0KeJIcP__wjdnY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}