@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4
> .
@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:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_head
{
this:
np:hasAssertion
dgn-np:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_assertion
;
np:hasProvenance
dgn-np:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_assertion
a
np:Assertion
.
dgn-np:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_provenance
a
np:Provenance
.
dgn-np:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0236642
a
ncit:C7057
.
dgn-gda:DGN0219de477cb2278f6684dd4a67cf2839
sio:SIO_000628
miriam-gene:4137
,
lld:C0236642
;
a
sio:SIO_001121
.
}
dgn-np:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_provenance
{
dgn-np:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_assertion
dcterms:description
"[Although our findings do not entirely exclude a mutation in a yet unanalyzed region of MAPT, the apparent absence of MAPT mutations combined with the lack of tau pathology is highly suggestive for another defective gene at 17q21 responsible for FTD in this family.]. 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:12476321
;
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:NP377349.RAZOUp3MLQNEw0cW6vYW5CXgY4qbIt65S9TJBdqiILbZ4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:36+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" .
}