@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo
> .
@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:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_head
{
this:
np:hasAssertion
dgn-np:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_assertion
;
np:hasProvenance
dgn-np:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_provenance
;
np:hasPublicationInfo
dgn-np:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_assertion
a
np:Assertion
.
dgn-np:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_provenance
a
np:Provenance
.
dgn-np:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_assertion
{
miriam-gene:3853
a
ncit:C16612
.
lld:C0265334
a
ncit:C7057
.
dgn-gda:DGNc9bec45bf429986dcaba9740fc2ea49c
sio:SIO_000628
miriam-gene:3853
,
lld:C0265334
;
a
sio:SIO_001121
.
}
dgn-np:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_provenance
{
dgn-np:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_assertion
dcterms:description
"[Targeting the single-nucleotide keratin 6a (K6a) N171K mutation responsible for the rare monogenic skin disorder pachyonychia congenita (PC), we demonstrate that small interfering RNAs (siRNAs) can potently and selectively block expression of mutant K6a.]. 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:17914454
;
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:NP419429.RA4aaJ0dUwQghuNhDdjC-m_ag0y_LpTUxqeqsf8rmyyCo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}