@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw
> .
@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:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_head
{
this:
np:hasAssertion
dgn-np:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_assertion
;
np:hasProvenance
dgn-np:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_provenance
;
np:hasPublicationInfo
dgn-np:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_assertion
a
np:Assertion
.
dgn-np:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_provenance
a
np:Provenance
.
dgn-np:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_assertion
{
miriam-gene:2312
a
ncit:C16612
.
lld:C0013595
a
ncit:C7057
.
dgn-gda:DGN0305e7ccc8bb00d67ef39c8a6235f143
sio:SIO_000628
miriam-gene:2312
,
lld:C0013595
;
a
sio:SIO_001121
.
}
dgn-np:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_provenance
{
dgn-np:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_assertion
dcterms:description
"[The association of filaggrin mutations with atopic eczema (atopic dermatitis, AD) is well established and it is thought that filaggrin dysfunction impairs the skin's barrier function allowing allergen penetration and subsequent cutaneous sensitisation and inflammation.]. 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:20975288
;
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:NP847989.RABB9PugHqNFWqiYf_k6RLW3J45gGcTCs3WN5bFifwXSw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:09+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: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" .
}