@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg
> .
@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:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_head
{
this:
np:hasAssertion
dgn-np:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_assertion
;
np:hasProvenance
dgn-np:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_provenance
;
np:hasPublicationInfo
dgn-np:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_assertion
a
np:Assertion
.
dgn-np:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_provenance
a
np:Provenance
.
dgn-np:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0003537
a
ncit:C7057
.
dgn-gda:DGNae5844d098c7313aa43a0adcf7b2e37b
sio:SIO_000628
miriam-gene:348
,
lld:C0003537
;
a
sio:SIO_001122
.
}
dgn-np:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_provenance
{
dgn-np:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_assertion
dcterms:description
"[On admission, there was no significant difference in the FIM or NIHSS measurements between the apo E4 group and other patients, but the prevalence of aphasia was 2.07 times more frequent in those with the APOE*E4 genotype (95% confidence interval, 0.98-4.4).]. 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:12881819
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP97908.RAW0r39Pb22COrz2BrqwXLtFcqy9nkinnS7IV2GqbBqzg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:34+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}