@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw
> .
@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 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:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_head
{
this:
np:hasAssertion
dgn-np:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_assertion
;
np:hasProvenance
dgn-np:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_assertion
a
np:Assertion
.
dgn-np:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_provenance
a
np:Provenance
.
dgn-np:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0085220
a
ncit:C7057
.
dgn-gda:DGNcff89364ce3ce8517298ae5401d297c8
sio:SIO_000628
miriam-gene:348
,
lld:C0085220
;
a
sio:SIO_001121
.
}
dgn-np:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_provenance
{
dgn-np:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_assertion
dc:description
"[possession of epsilon4 does not by itself confer an increased risk of cerebral amyloid angiopathy but may be associated with reduced longevity even in the absence of alzheimer's disease or cerebral haemorrhage ]. 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:12960780
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP128044.RAhEbAWPlWJV0HneNGxDrhUrqvlVkYvSEC3AwgXyPVDFw130_publicationInfo
{
this:
dc:created
"2014-10-02T12:33:06+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}