@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac
> .
@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:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_head
{
this:
np:hasAssertion
dgn-np:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_assertion
;
np:hasProvenance
dgn-np:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_provenance
;
np:hasPublicationInfo
dgn-np:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_assertion
a
np:Assertion
.
dgn-np:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_provenance
a
np:Provenance
.
dgn-np:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_assertion
{
miriam-gene:1041
a
ncit:C16612
.
lld:C1849193
a
ncit:C7057
.
dgn-gda:DGN7330d473a894bafaea740965f5004ca7
sio:SIO_000628
miriam-gene:1041
,
lld:C1849193
;
a
sio:SIO_001121
.
}
dgn-np:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_provenance
{
dgn-np:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_assertion
dcterms:description
"[Genetic defects in corneodesmosin and inhibitors for proteases involved in corneodesmosome degradation result in accelerated desquamation and severe barrier impairment, presenting as the inflammatory type of peeling skin syndrome and Netherton syndrome, respectively.]. 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:21545505
;
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:NP347235.RAx7Cjpkjjd-KAw47HJN71x0xhAAmOtVjTeOI116k30ac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:24+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" .
}