@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ
> .
@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:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_head
{
this:
np:hasAssertion
dgn-np:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_assertion
;
np:hasProvenance
dgn-np:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_assertion
a
np:Assertion
.
dgn-np:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_provenance
a
np:Provenance
.
dgn-np:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_assertion
{
miriam-gene:23435
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNd48e16c0ec5b9e50da42b9713367f074
sio:SIO_000628
miriam-gene:23435
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_provenance
{
dgn-np:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_assertion
dcterms:description
"[This study defined the distribution and frequency of mutations of FALS in a Taiwanese Han Chinese population, which not only broadens the spectrum of the mutations causing FALS, but also further highlights the importance of FUS and TARDBP in the pathogenesis of amyotrophic lateral sclerosis (ALS).]. 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:20472325
;
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:NP812303.RAPgFM0Dg-u2beU1SZCjghyGOL6zhbaPNWb1IdncquSWQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:53+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" .
}