@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk
> .
@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:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_head
{
this:
np:hasAssertion
dgn-np:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_assertion
;
np:hasProvenance
dgn-np:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_provenance
;
np:hasPublicationInfo
dgn-np:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_assertion
a
np:Assertion
.
dgn-np:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_provenance
a
np:Provenance
.
dgn-np:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_assertion
{
miriam-gene:5317
a
ncit:C16612
.
lld:C0013575
a
ncit:C7057
.
dgn-gda:DGNce602154d2077463503910b0863ad420
sio:SIO_000628
miriam-gene:5317
,
lld:C0013575
;
a
sio:SIO_001121
.
}
dgn-np:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_provenance
{
dgn-np:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_assertion
dcterms:description
"[In addition, a rare autosomal recessive skin fragility-ectodermal dysplasia syndrome has recently been recognised which results from total ablation of plakophilin 1, an intracellular desmosomal plaque protein that reinforces adhesion between the cytoskeleton and the cell membrane in terminally differentiating keratinocytes.]. 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:10379701
;
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:NP635768.RA8upLqgYnQdwFf4b91ZbFBjasl-KpNKyx9hotULegdzk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}