@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI
> .
@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:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_head
{
this:
np:hasAssertion
dgn-np:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_assertion
;
np:hasProvenance
dgn-np:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_provenance
;
np:hasPublicationInfo
dgn-np:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_assertion
a
np:Assertion
.
dgn-np:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_provenance
a
np:Provenance
.
dgn-np:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_assertion
{
miriam-gene:3596
a
ncit:C16612
.
lld:C0011615
a
ncit:C7057
.
dgn-gda:DGN10842d68c78caf80a954b88897027a3c
sio:SIO_000628
miriam-gene:3596
,
lld:C0011615
;
a
sio:SIO_001122
.
}
dgn-np:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_provenance
{
dgn-np:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_assertion
dcterms:description
"[This result suggests that 4257A allele is associated with susceptibility to AD and that it may function in the pathogenesis of AD itself, presumably by other mechanisms than inducing IgE production.]. 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:12413765
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP56630.RAiFY5ZoYpphU4lFrmdWU943TBRmylMQupVEoQHI5NQeI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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" .
}