@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ
> .
@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:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_head
{
this:
np:hasAssertion
dgn-np:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_assertion
;
np:hasProvenance
dgn-np:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_assertion
a
np:Assertion
.
dgn-np:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_provenance
a
np:Provenance
.
dgn-np:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_assertion
{
miriam-gene:2260
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN99f1b7e7d6809e5ab973aaa6cf4182f2
sio:SIO_000628
miriam-gene:2260
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_provenance
{
dgn-np:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_assertion
dcterms:description
"[In the Polish patients with AD, the prevalence of FLG mutations was higher in patients with AD than in the controls and 2282del4 FLG mutation was more frequent than R501X, and it was associated with a 6-fold higher risk for AD development (P < 0.001; OR: 5.76), moderate or severe disease course, early onset of asthma and palmar hyperlinearity.]. 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:21426411
;
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:NP406419.RAbe6wW9djTjXCW9d8M7Wr6zn1LqN-R_CHHu8_ro_TRDQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:02+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" .
}