@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4
> .
@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:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_head
{
this:
np:hasAssertion
dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_assertion
;
np:hasProvenance
dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_provenance
;
np:hasPublicationInfo
dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_assertion
a
np:Assertion
.
dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_provenance
a
np:Provenance
.
dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_assertion
{
miriam-gene:2260
a
ncit:C16612
.
lld:C0037274
a
ncit:C7057
.
dgn-gda:DGNade2c370747a279e685bd8900f4faf8c
sio:SIO_000628
miriam-gene:2260
,
lld:C0037274
;
a
sio:SIO_001121
.
}
dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_provenance
{
dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_assertion
dcterms:description
"[This review aims to summarize the current state of knowledge regarding the role of FLG mutations in ichthyosis vulgaris, atopic eczema, and other skin disorders, with an emphasis on potential clinical applications.]. 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:18620134
;
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:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:40+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" .
}