@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg
> .
@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:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_head
{
this:
np:hasAssertion
dgn-np:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_assertion
;
np:hasProvenance
dgn-np:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_provenance
;
np:hasPublicationInfo
dgn-np:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_assertion
a
np:Assertion
.
dgn-np:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_provenance
a
np:Provenance
.
dgn-np:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_assertion
{
miriam-gene:2312
a
ncit:C16612
.
lld:C0079588
a
ncit:C7057
.
dgn-gda:DGNea23d0d66b4fe7e6f1d53436572e9ed1
sio:SIO_000628
miriam-gene:2312
,
lld:C0079588
;
a
sio:SIO_001121
.
}
dgn-np:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_provenance
{
dgn-np:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_assertion
dcterms:description
"[This is the second reported case of the modifying effects of FLG null alleles on XLI and strengthens the hypothesis that filaggrin defects can synergize with STS deficiency to exacerbate the ichthyosis phenotype.]. 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:21945601
;
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:NP598339.RAVSkSZMnwEcaF_jE6m3XL_MPU7G2eX8E1hVkrSJ6NwKg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}