@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM
> .
@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:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_head
{
this:
np:hasAssertion
dgn-np:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_assertion
;
np:hasProvenance
dgn-np:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_provenance
;
np:hasPublicationInfo
dgn-np:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_assertion
a
np:Assertion
.
dgn-np:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_provenance
a
np:Provenance
.
dgn-np:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0038868
a
ncit:C7057
.
dgn-gda:DGN148736f088fc1465906cce6668778d1a
sio:SIO_000628
miriam-gene:4137
,
lld:C0038868
;
a
sio:SIO_001121
.
}
dgn-np:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_provenance
{
dgn-np:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_assertion
dcterms:description
"[However, in the sporadic tauopathies such as progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) where MAPT mutation is absent, common variation in MAPT that defines the H1 and H2 haplotype clades strongly influences disease risk.]. 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:20704554
;
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:NP832355.RAcvuLosIfXEgURqEzKV2usUwo1aMFtGRo2C5DzHY0lQM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:02+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" .
}