@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM
> .
@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:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_head
{
this:
np:hasAssertion
dgn-np:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_assertion
;
np:hasProvenance
dgn-np:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_provenance
;
np:hasPublicationInfo
dgn-np:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_assertion
a
np:Assertion
.
dgn-np:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_provenance
a
np:Provenance
.
dgn-np:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_assertion
{
miriam-gene:2312
a
ncit:C16612
.
lld:C0020725
a
ncit:C7057
.
dgn-gda:DGNd45913569888dd6da7bfd6f1e6db8e26
sio:SIO_000628
miriam-gene:2312
,
lld:C0020725
;
a
sio:SIO_001121
.
}
dgn-np:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_provenance
{
dgn-np:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_assertion
dcterms:description
"[The most important development has been the discovery that loss-of-function mutations in the gene encoding the epidermal protein filaggrin increase the risk for ICD and for nickel sensitization and nickel ACD, emphasizing the importance of the skin barrier in the pathophysiology of CD.]. 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:21329569
;
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:NP861044.RAmeaNdDSwStXAkn63BLlk1S95BiWqykKMlqQjz7EKGDM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:46+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" .
}