@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk
> .
@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:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_head
{
this:
np:hasAssertion
dgn-np:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_assertion
;
np:hasProvenance
dgn-np:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_assertion
a
np:Assertion
.
dgn-np:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_provenance
a
np:Provenance
.
dgn-np:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0751265
a
ncit:C7057
.
dgn-gda:DGNd4cb8b64bac74d3eee1feca302f7c226
sio:SIO_000628
miriam-gene:4137
,
lld:C0751265
;
a
sio:SIO_001121
.
}
dgn-np:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_provenance
{
dgn-np:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_assertion
dcterms:description
"[The MAPT H1 haplotype has been associated with progressive supranuclear palsy, corticobasal degeneration, Parkinson's disease and Alzheimer's disease, while the H2 is linked to recurrent deletion events associated with the 17q21.31 microdeletion syndrome, a disease characterized by developmental delay and learning disability.]. 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:22950410
;
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:NP1010437.RAlya3GnBhmT7_c5uHxlRcS-4jWw9BTpasYfD-MpMVmtk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:23+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" .
}