@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk
> .
@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:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_head
{
this:
np:hasAssertion
dgn-np:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_assertion
;
np:hasProvenance
dgn-np:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance
;
np:hasPublicationInfo
dgn-np:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_assertion
a
np:Assertion
.
dgn-np:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance
a
np:Provenance
.
dgn-np:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_assertion
{
miriam-gene:2705
a
ncit:C16612
.
lld:C0004093
a
ncit:C7057
.
dgn-gda:DGN50ba50000a7a5627c402fe57be5051f0
sio:SIO_000628
miriam-gene:2705
,
lld:C0004093
;
a
sio:SIO_001121
.
}
dgn-np:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance
{
dgn-np:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_assertion
dcterms:description
"[Two brothers with no copy of Cx32, 27 and 25 years old, showed steppage gait, moderate muscle atrophy and weakness, and mild sensory disturbance in the distal parts of the legs.]. 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:11266688
;
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:NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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" .
}