@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_head
{
this:
np:hasAssertion
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_assertion
;
np:hasProvenance
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_provenance
;
np:hasPublicationInfo
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_assertion
a
np:Assertion
.
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_provenance
a
np:Provenance
.
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0393570
a
ncit:C7057
.
dgn-gda:DGN9c5b092b94af479aeec7a313944cf90a
sio:SIO_000628
miriam-gene:4137
,
lld:C0393570
;
a
sio:SIO_001121
.
}
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_provenance
{
dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_assertion
dcterms:description
"[The MAPT (microtubule-associated protein tau) locus is one of the most remarkable in neurogenetics due not only to its involvement in multiple neurodegenerative disorders, including progressive supranuclear palsy, corticobasal degeneration, Parksinson's disease and possibly Alzheimer's disease, but also due its genetic evolution and complex alternative splicing features which are, to some extent, linked and so all the more intriguing.]. 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:22723018
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:43+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}