@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w
> .
@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:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_head
{
this:
np:hasAssertion
dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_assertion
;
np:hasProvenance
dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_provenance
;
np:hasPublicationInfo
dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_assertion
a
np:Assertion
.
dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_provenance
a
np:Provenance
.
dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0038868
a
ncit:C7057
.
dgn-gda:DGN260661d280ce2c37a05ee84ca0d19550
sio:SIO_000628
miriam-gene:4137
,
lld:C0038868
;
a
sio:SIO_001121
.
}
dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_provenance
{
dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_assertion
dcterms:description
"[Recent studies have reported high familial aggregation in PSP patients, and it has been widely demonstrated that Microtuble Associated Protein Tau (MAPT) gene mutations are causative of monogenic autosomal dominant PSP.]. 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:21568901
;
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:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:29+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" .
}