@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw
> .
@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/v3.0.0/void/
> .
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_head
{
this:
np:hasAssertion
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_assertion
;
np:hasProvenance
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_provenance
;
np:hasPublicationInfo
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_assertion
a
np:Assertion
.
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_provenance
a
np:Provenance
.
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_assertion
{
miriam-gene:2312
a
ncit:C16612
.
lld:C0022504
a
ncit:C7057
.
dgn-gda:DGN84bae2bccf636bfc04c2a0a3804ad26d
sio:SIO_000628
miriam-gene:2312
,
lld:C0022504
;
a
sio:SIO_001122
.
}
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_provenance
{
dgn-np:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_assertion
dcterms:description
"[The R501X mutation in the gene encoding filaggrin, one of the strongest genetic predictors of AD, confers an even greater risk for ADEH in both European and African ancestry populations, suggesting a role for defective skin barrier in this devastating con]. 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:19733298
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP107317.RAnoxcnpGK48NfCljIe3dUWU8Q_qMSt9eg4N38Fpug0qw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:39+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}