@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8
> .
@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:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_head
{
this:
np:hasAssertion
dgn-np:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_assertion
;
np:hasProvenance
dgn-np:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_provenance
;
np:hasPublicationInfo
dgn-np:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_assertion
a
np:Assertion
.
dgn-np:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_provenance
a
np:Provenance
.
dgn-np:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_assertion
{
miriam-gene:3858
a
ncit:C16612
.
lld:C0037274
a
ncit:C7057
.
dgn-gda:DGNeac769402905393ed9fa637ccea38e4c
sio:SIO_000628
miriam-gene:3858
,
lld:C0037274
;
a
sio:SIO_001121
.
}
dgn-np:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_provenance
{
dgn-np:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_assertion
dcterms:description
"[The expression of mutant keratin genes has produced animal models of epidermolysis bullosa simplex and epidermolytic hyperkeratosis and, in doing so, has focused attention on the genetics of keratins in these and other skin disorders.]. 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:7694550
;
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:NP824714.RA5XoQAF0v_8NAQIxgs5sVEl1EmEeqF4Fo7W9kKRQr0g8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}