@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo
> .
@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:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_head
{
this:
np:hasAssertion
dgn-np:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_assertion
;
np:hasProvenance
dgn-np:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_provenance
;
np:hasPublicationInfo
dgn-np:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_assertion
a
np:Assertion
.
dgn-np:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_provenance
a
np:Provenance
.
dgn-np:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0393570
a
ncit:C7057
.
dgn-gda:DGN46a8ac11c890c96cf260089b8b40f82e
sio:SIO_000628
miriam-gene:4137
,
lld:C0393570
;
a
sio:SIO_001121
.
}
dgn-np:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_provenance
{
dgn-np:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_assertion
dcterms:description
"[Previously we have shown that the H1c haplotype on the background of the H1 clade of haplotypes at the MAPT locus is associated with increased risk for progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and Alzheimer's disease (AD).]. 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:17174556
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP546175.RAFRCyy6dKyLpW4YVML1dshLauNM-u1C_icWYF-gUoGgo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:03+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" .
}