@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI
> .
@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:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_head
{
this:
np:hasAssertion
dgn-np:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_assertion
;
np:hasProvenance
dgn-np:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_provenance
;
np:hasPublicationInfo
dgn-np:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_assertion
a
np:Assertion
.
dgn-np:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_provenance
a
np:Provenance
.
dgn-np:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_assertion
{
miriam-gene:3857
a
ncit:C16612
.
lld:C0870082
a
ncit:C7057
.
dgn-gda:DGN8cd2df28d8d39877d460617aff27f75b
sio:SIO_000628
miriam-gene:3857
,
lld:C0870082
;
a
sio:SIO_001121
.
}
dgn-np:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_provenance
{
dgn-np:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_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-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:NP822001.RAnJ1jNHkpBg6qI7YzspwqRFqpyG6Q2A5VO_M1vOx9ErI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}