@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8
> .
@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:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_head
{
this:
np:hasAssertion
dgn-np:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_assertion
;
np:hasProvenance
dgn-np:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_provenance
;
np:hasPublicationInfo
dgn-np:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_assertion
a
np:Assertion
.
dgn-np:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_provenance
a
np:Provenance
.
dgn-np:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_assertion
{
miriam-gene:7052
a
ncit:C16612
.
lld:C0544008
a
ncit:C7057
.
dgn-gda:DGN0f367ef1ea26214ee05d983490adf8a6
sio:SIO_000628
miriam-gene:7052
,
lld:C0544008
;
a
sio:SIO_001121
.
}
dgn-np:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_provenance
{
dgn-np:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_assertion
dcterms:description
"[We tested for an association between an intronic TGC trinucleotide repeat in TCF4 and FECD by determining repeat length in 66 affected participants with severe FECD and 63 participants with normal corneas in a 3-stage discovery/replication/validation study.]. 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:23185296
;
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:NP181292.RA2PAeX7156250yamLqvOxnD3BcHdJqaBHC1jhZXF4iA8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}