@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI
> .
@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:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_head
{
this:
np:hasAssertion
dgn-np:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_assertion
;
np:hasProvenance
dgn-np:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_provenance
;
np:hasPublicationInfo
dgn-np:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_assertion
a
np:Assertion
.
dgn-np:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_provenance
a
np:Provenance
.
dgn-np:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_assertion
{
miriam-gene:2
a
ncit:C16612
.
lld:C0494463
a
ncit:C7057
.
dgn-gda:DGN8ef4f6be44dd7b82be639c69feb7febc
sio:SIO_000628
miriam-gene:2
,
lld:C0494463
;
a
sio:SIO_001121
.
}
dgn-np:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_provenance
{
dgn-np:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_assertion
dcterms:description
"[As recently it has been suggested that the effect of the A2M gene on AD susceptibility may be limited to certain populations or families, we analyzed the segregation of A2M and apolipoprotein E polymorphisms in Italian sporadic and familial AD.]. 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:11166925
;
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:NP595687.RA4qw0sssuqiitJ6aSycCpueoIbdGtCZ4RQxE5mmcg1CI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:58+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" .
}