@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI
> .
@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:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_head
{
this:
np:hasAssertion
dgn-np:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_assertion
;
np:hasProvenance
dgn-np:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_provenance
;
np:hasPublicationInfo
dgn-np:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_assertion
a
np:Assertion
.
dgn-np:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_provenance
a
np:Provenance
.
dgn-np:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C1883552
a
ncit:C7057
.
dgn-gda:DGN95e60575ce39d39a2ee72ba82d030533
sio:SIO_000628
miriam-gene:367
,
lld:C1883552
;
a
sio:SIO_001121
.
}
dgn-np:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_provenance
{
dgn-np:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_assertion
dcterms:description
"[A rare, predominantly distal distribution of weakness and amyotrophy was found in our group of the SBMA patients (8 out of 11 cases) from three unrelated kindreds and also in the remaining two sporadic cases.]. 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:16753970
;
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:NP818830.RAke89gzlOY-uwO8uke1qUHoXI44GgD0ExHp9RtKC5OFI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:21+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" .
}