@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ
> .
@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/v4.0.0/void/
> .
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_head
{
this:
np:hasAssertion
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_assertion
;
np:hasProvenance
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_assertion
a
np:Assertion
.
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_provenance
a
np:Provenance
.
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGN96598d6716151316823552d9ea5dba7e
sio:SIO_000628
miriam-gene:348
,
lld:C0497327
;
a
sio:SIO_001121
.
}
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_provenance
{
dgn-np:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_assertion
dcterms:description
"[However, no change in the frequency of ApoE alleles was found in two of the clinical and pathological forms of LA (dementia of frontal type and dementia of frontal type with motor neurone disease) although the ApoE E4 allele frequency was elevated in cases of non-fluent progressive aphasia in accordance with the presence of coincidental Alzheimer-type pathological changes.]. 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:7609910
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1314973.RA-2PokjtZxBvo2WUn1E7ge_GZv77PwddymYoSuRSvxyQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:42+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}