@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY
> .
@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:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_head
{
this:
np:hasAssertion
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_assertion
;
np:hasProvenance
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_provenance
;
np:hasPublicationInfo
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_assertion
a
np:Assertion
.
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_provenance
a
np:Provenance
.
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_assertion
{
miriam-gene:3858
a
ncit:C16612
.
lld:C0037274
a
ncit:C7057
.
dgn-gda:DGN49546a379f6e0d7d115e3f2c32b5798f
sio:SIO_000628
miriam-gene:3858
,
lld:C0037274
;
a
sio:SIO_001121
.
}
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_provenance
{
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_assertion
dcterms:description
"[With the exciting discovery that three autosomal dominant genetic skin disorders, epidermolysis bullosa simplex (EBS), epidermolytic hyperkeratosis (EHK) and palmoplantar keratoderma (PPK), are in fact disorders of keratins comes the realization that the integrity of the keratin filament network is crucial to the structural integrity of the skin.]. 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:7528048
;
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:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}