@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_head
{
this:
np:hasAssertion
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_assertion
;
np:hasProvenance
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_provenance
;
np:hasPublicationInfo
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_assertion
a
np:Assertion
.
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_provenance
a
np:Provenance
.
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_assertion
{
miriam-gene:2312
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNd9255f0c0efd0158f437db8abf73757f
sio:SIO_000628
miriam-gene:2312
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_provenance
{
dgn-np:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP881517.RAiHBxJE1rD0m90iNpx9vWEUN8WDHEVpkkG1byebnpEDc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:24+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}