@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4
> .
@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:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_head
{
this:
np:hasAssertion
dgn-np:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_assertion
;
np:hasProvenance
dgn-np:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_provenance
;
np:hasPublicationInfo
dgn-np:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_assertion
a
np:Assertion
.
dgn-np:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_provenance
a
np:Provenance
.
dgn-np:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_assertion
{
miriam-gene:29978
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN29489adf30a932baa8ca331e5a75c4bd
sio:SIO_000628
miriam-gene:29978
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_provenance
{
dgn-np:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_assertion
dcterms:description
"[In particular, the progress in the molecular neuropathology with the discovery of pathogenic mutations in TAR DNA binding protein (TARDBP), fused in sarcoma (FUS), ubiquilin2 (UBQLN2) and most recently C9ORF72 (abbreviation for the open reading frame 72 on chromosome 9) has further substantiated the - clinically temporarily forgotten - relation of classic ALS to frontotemporal degeneration (FTD).]. 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:22918486
;
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:NP225438.RAqmxImt9mhO9pT2EXEfWnor7mhY7u6D4J1fpwf55fPL4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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: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" .
}