@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE
> .
@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:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_head
{
this:
np:hasAssertion
dgn-np:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_assertion
;
np:hasProvenance
dgn-np:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_assertion
a
np:Assertion
.
dgn-np:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_provenance
a
np:Provenance
.
dgn-np:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_assertion
{
miriam-gene:79623
a
ncit:C16612
.
lld:C2827407
a
ncit:C7057
.
dgn-gda:DGN1428b2ee00a57afaef616221db8c31e1
sio:SIO_000628
miriam-gene:79623
,
lld:C2827407
;
a
sio:SIO_001121
.
}
dgn-np:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_provenance
{
dgn-np:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_assertion
dcterms:description
"[This first discovery GWAS for an OM phenotype has identified CAPN14 and GALNT14 on chromosome 2p23.1 and the BPIFA gene cluster on chromosome 20q11.21 as novel candidate genes which warrant further analysis in cohorts matched more precisely for clinical phenotypes.]. 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:23133572
;
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:NP479809.RAgje9QCDKdVqG6RgkeuwlGsFPMWIYk83FsesvvX0bBGE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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" .
}