@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q
> .
@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:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_head
{
this:
np:hasAssertion
dgn-np:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_assertion
;
np:hasProvenance
dgn-np:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_assertion
a
np:Assertion
.
dgn-np:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_provenance
a
np:Provenance
.
dgn-np:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_assertion
{
miriam-gene:51164
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNcc536ed3ae7c254d41f4bfccdfa21680
sio:SIO_000628
miriam-gene:51164
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_provenance
{
dgn-np:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_assertion
dcterms:description
"[The purpose of this study was to find mutations in the SQSTM1 gene encoding p62 in Japanese patients with amyotrophic lateral sclerosis (ALS), since this gene has been recently identified as a causative gene for familial and sporadic ALS in the United States.]. 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:23303844
;
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:NP843536.RAOGgBA1bosh71E76wD5ZAS6euroC3v_v0pDK36husN7Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:35+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" .
}