@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw
> .
@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:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_head
{
this:
np:hasAssertion
dgn-np:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_assertion
;
np:hasProvenance
dgn-np:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_provenance
;
np:hasPublicationInfo
dgn-np:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_assertion
a
np:Assertion
.
dgn-np:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_provenance
a
np:Provenance
.
dgn-np:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_assertion
{
miriam-gene:79983
a
ncit:C16612
.
lld:C0025322
a
ncit:C7057
.
dgn-gda:DGNb288495e83ac8d9deb674b6e421822ca
sio:SIO_000628
miriam-gene:79983
,
lld:C0025322
;
a
sio:SIO_001121
.
}
dgn-np:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_provenance
{
dgn-np:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_assertion
dcterms:description
"[The tight junction localisation was maintained by the human POF1B stably expressed in the MDCK polarised epithelial cell line, whereas it was lost by the POF1B R329Q variant associated 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:21940798
;
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:NP824698.RA71EI0r7Yc5_sZc3F2zeCyeWL6aqgpHP3GjEjbhvIlUw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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: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" .
}