@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ
> .
@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:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_head
{
this:
np:hasAssertion
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_assertion
;
np:hasProvenance
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_assertion
a
np:Assertion
.
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_provenance
a
np:Provenance
.
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_assertion
{
miriam-gene:3553
a
ncit:C16612
.
lld:C0276496
a
ncit:C7057
.
dgn-gda:DGN9ef06e5d4461c2154575d4c3594a958b
sio:SIO_000628
miriam-gene:3553
,
lld:C0276496
;
a
sio:SIO_001121
.
}
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_provenance
{
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_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-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:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}