@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg
> .
@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/v3.0.0/void/
> .
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_head
{
this:
np:hasAssertion
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_assertion
;
np:hasProvenance
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance
;
np:hasPublicationInfo
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_assertion
a
np:Assertion
.
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance
a
np:Provenance
.
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_assertion
{
miriam-gene:2705
a
ncit:C16612
.
lld:C3714552
a
ncit:C7057
.
dgn-gda:DGN5ba29883bf0f209eb4e977eda6138394
sio:SIO_000628
miriam-gene:2705
,
lld:C3714552
;
a
sio:SIO_001121
.
}
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_provenance
{
dgn-np:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP426228.RAAUU9EiYQwbA1iK-nSGiRz3322-AB0dHA37TYccK5PSg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:48+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}