@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg
> .
@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/v3.0.0/void/
> .
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_head
{
this:
np:hasAssertion
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_assertion
a
np:Assertion
.
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_provenance
a
np:Provenance
.
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0276496
a
ncit:C7057
.
dgn-gda:DGN3686cc34d4f2297aa0e830838e56f488
sio:SIO_000628
miriam-gene:348
,
lld:C0276496
;
a
sio:SIO_001121
.
}
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_provenance
{
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_assertion
dcterms:description
"[For the more common sporadic forms of AD, increased risk has been associated with a number of genes; the most important of which is the epsilon4 allele of apolipoprotein E. Two recent studies, one clinical and one using postmortem material, now show increased risk for AD associated with certain polymorphisms in the genes encoding the alpha and beta isoforms of interleukin-1 (IL-1).]. 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:10850859
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:00+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
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;
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
}