@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU
> .
@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:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_head
{
this:
np:hasAssertion
dgn-np:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_assertion
;
np:hasProvenance
dgn-np:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance
;
np:hasPublicationInfo
dgn-np:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_assertion
a
np:Assertion
.
dgn-np:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance
a
np:Provenance
.
dgn-np:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0949664
a
ncit:C7057
.
dgn-gda:DGN10c9cd958df50078db98cc7876eec7ee
sio:SIO_000628
miriam-gene:4137
,
lld:C0949664
;
a
sio:SIO_001121
.
}
dgn-np:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_provenance
{
dgn-np:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_assertion
dcterms:description
"[However, since specific polymorphisms and mutations in the tau gene lead to diverse phenotypes, it is plausible that additional genetic or epigenetic factors influence the clinical and pathological manifestations of both familial and sporadic tauopathies.]. 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:11207421
;
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:NP308558.RABSoIhU2vmXLxAgPxrMgzUFzWb3fvXtDIeWVCgAK2IuU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:05+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" .
}