@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA
> .
@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:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_head
{
this:
np:hasAssertion
dgn-np:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_assertion
;
np:hasProvenance
dgn-np:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_provenance
;
np:hasPublicationInfo
dgn-np:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_assertion
a
np:Assertion
.
dgn-np:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_provenance
a
np:Provenance
.
dgn-np:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_assertion
{
miriam-gene:2260
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN772b3de869109b877a7f15d134a19091
sio:SIO_000628
miriam-gene:2260
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_provenance
{
dgn-np:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_assertion
dcterms:description
"[Our results suggest that FLG mutations are key organ specific factors predominantly affecting the development of eczema and confer significant risks of allergic sensitization and allergic rhinitis as well as asthma in the context of eczema.]. 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:18396323
;
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:NP186341.RAGI2Ls7YOimXLy0SUAdbhzrE5LcJtMuHhxhKoQrUhItA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}