@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_head
{
this:
np:hasAssertion
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_assertion
;
np:hasProvenance
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_provenance
;
np:hasPublicationInfo
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_assertion
a
np:Assertion
.
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_provenance
a
np:Provenance
.
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_assertion
{
miriam-gene:3861
a
ncit:C16612
.
lld:C0079298
a
ncit:C7057
.
dgn-gda:DGN6ac97509e4a3876b7bd5cde22547a463
sio:SIO_000628
miriam-gene:3861
,
lld:C0079298
;
a
sio:SIO_001121
.
}
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_provenance
{
dgn-np:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_assertion
dcterms:description
"[Epidermolysis bullosa simplex (EBS) is an inherited skin disorder caused by mutations in keratins K5 (keratin 5) and K14 (keratin 14), with fragility of basal keratinocytes leading to epidermal cytolysis and blistering.]. 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:17039244
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP574110.RADcJhnZKormQqknTUhlMiJpMR0HDO7Yd40ATETQlbdPM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:05+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}