@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q
> .
@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:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_head
{
this:
np:hasAssertion
dgn-np:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_assertion
;
np:hasProvenance
dgn-np:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_assertion
a
np:Assertion
.
dgn-np:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_provenance
a
np:Provenance
.
dgn-np:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_assertion
{
miriam-gene:3857
a
ncit:C16612
.
lld:C0022596
a
ncit:C7057
.
dgn-gda:DGNdf5f652ee5771ba94954384d1155d0dc
sio:SIO_000628
miriam-gene:3857
,
lld:C0022596
;
a
sio:SIO_001121
.
}
dgn-np:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_provenance
{
dgn-np:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_assertion
dcterms:description
"[These findings provide further evidence that mutations in keratin genes may cause epidermolysis and hyperkeratosis and that hyperkeratosis of palms and soles may be caused by different mutations in the KRT9 gene.]. 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:7512862
;
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:NP1309677.RAknc7PQzfHGrRBLlEUkxfn-BT80eYyEWf8DfMAwqg09Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:39+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" .
}