@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI
> .
@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:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_head
{
this:
np:hasAssertion
dgn-np:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_assertion
;
np:hasProvenance
dgn-np:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_provenance
;
np:hasPublicationInfo
dgn-np:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_assertion
a
np:Assertion
.
dgn-np:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_provenance
a
np:Provenance
.
dgn-np:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_assertion
{
miriam-gene:2312
a
ncit:C16612
.
lld:C0239816
a
ncit:C7057
.
dgn-gda:DGNc981dd255f21abf8c51444b955258d06
sio:SIO_000628
miriam-gene:2312
,
lld:C0239816
;
a
sio:SIO_001121
.
}
dgn-np:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_provenance
{
dgn-np:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_assertion
dcterms:description
"[In our clinic, we have observed a distinct phenotype of hand eczema in patients with filaggrin mutation carrier status, characterized by fissured dermatitis on the dorsal aspect of the hands and with only sparse involvement of the palms including fine scaling.]. 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:21777221
;
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:NP252328.RAydCc6UWdATvzBEwh2ivYCfbvL7bG2CycRJmU1ioMfzI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:21+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" .
}