@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA
> .
@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:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_head
{
this:
np:hasAssertion
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_assertion
;
np:hasProvenance
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_provenance
;
np:hasPublicationInfo
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_assertion
a
np:Assertion
.
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_provenance
a
np:Provenance
.
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_assertion
{
miriam-gene:3858
a
ncit:C16612
.
lld:C0037274
a
ncit:C7057
.
dgn-gda:DGNec93df8c5b855e87f26f368f48d14370
sio:SIO_000628
miriam-gene:3858
,
lld:C0037274
;
a
sio:SIO_001121
.
}
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_provenance
{
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_assertion
dcterms:description
"[Analyzing keratin gene sequences, appreciating the switch in keratin gene expression that takes place as epidermal cells commit to terminally differentiate, and elucidating how keratins assemble into 10 nm filaments, have provided the foundation that has led to the discoveries of the genetic bases of two major classes of human skin diseases, epidermolysis bullosa simplex (EBS) and epidermolytic hyperkeratosis (EH).]. 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:7520042
;
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:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}