@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY
> .
@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:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_head
{
this:
np:hasAssertion
dgn-np:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_assertion
;
np:hasProvenance
dgn-np:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_provenance
;
np:hasPublicationInfo
dgn-np:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_assertion
a
np:Assertion
.
dgn-np:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_provenance
a
np:Provenance
.
dgn-np:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_assertion
{
miriam-gene:3857
a
ncit:C16612
.
lld:C0037277
a
ncit:C7057
.
dgn-gda:DGNea05c85532e6d02efb6505f538d8e712
sio:SIO_000628
miriam-gene:3857
,
lld:C0037277
;
a
sio:SIO_001121
.
}
dgn-np:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_provenance
{
dgn-np:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_assertion
dcterms:description
"[Epidermolytic palmoplantar keratoderma (EPPK) is an autosomal dominant genodermatosis characterized by epidermolytic hyperkeratosis strictly confined to the palms and soles, and usually associated with mutations in the keratin K9 gene (KRT9).]. 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:15214894
;
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:NP214155.RAIqWAj_Wi-QJtAmOl9jBzm6cHZXVWhZj3JN9w0yAJJFY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}