@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4
> .
@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:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_head
{
this:
np:hasAssertion
dgn-np:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_assertion
;
np:hasProvenance
dgn-np:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_provenance
;
np:hasPublicationInfo
dgn-np:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_assertion
a
np:Assertion
.
dgn-np:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_provenance
a
np:Provenance
.
dgn-np:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN208d21c99d3334112953636b9678028f
sio:SIO_000628
miriam-gene:348
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_provenance
{
dgn-np:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_assertion
dcterms:description
"[The polymorphism of apolipoprotein E (apoE) has been recognized as a genetic risk factor in different neurodegenerative disorders, with or without tau protein- related neuropathology, but few published epidemiological data are available as concerns the association of different apoE alleles with two relatively rare forms of dementia, Pick's disease (PiD) and Huntington's disease (HD).]. 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:10924769
;
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:NP310669.RAJPYn2FAvWzMW_kvcn4EAVrkDuvOkqtuS9FfNBGls_d4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:58+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" .
}