@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0
> .
@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:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_head
{
this:
np:hasAssertion
dgn-np:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_assertion
;
np:hasProvenance
dgn-np:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_provenance
;
np:hasPublicationInfo
dgn-np:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_assertion
a
np:Assertion
.
dgn-np:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_provenance
a
np:Provenance
.
dgn-np:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_assertion
{
miriam-gene:2312
a
ncit:C16612
.
lld:C0162823
a
ncit:C7057
.
dgn-gda:DGN2754faf30da43e648f7878908b3a70c5
sio:SIO_000628
miriam-gene:2312
,
lld:C0162823
;
a
sio:SIO_001121
.
}
dgn-np:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_provenance
{
dgn-np:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_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-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:NP873263.RAm_jJgGqhVuhmiLsoj9s-oq4WQyMLSVVFhtMuAb3tBW0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:20+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" .
}