@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4
> .
@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:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_head
{
this:
np:hasAssertion
dgn-np:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_assertion
;
np:hasProvenance
dgn-np:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_provenance
;
np:hasPublicationInfo
dgn-np:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_assertion
a
np:Assertion
.
dgn-np:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_provenance
a
np:Provenance
.
dgn-np:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_assertion
{
miriam-gene:26580
a
ncit:C16612
.
lld:C0037771
a
ncit:C7057
.
dgn-gda:DGNed7b242bc3783e7d9076d1212f3fceaa
sio:SIO_000628
miriam-gene:26580
,
lld:C0037771
;
a
sio:SIO_001121
.
}
dgn-np:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_provenance
{
dgn-np:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_assertion
dcterms:description
"[The clinical patterns in this family include presentation with lower-limb and hand-muscle involvement early in the disease course as well as the presence of Babinski signs with nonprogressive mild spastic paraparesis, resembling classic Silver syndrome and dHMN type V. This study reaffirms the clinical phenotype of the disorders associated with a BSCL2 Ser90Leu mutation and describes a genetically proven family with Silver syndrome and dHMN type V in Asia.]. 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:17486577
;
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:NP233589.RAQqJikBosMhnGfcyF95o6lUQ8mGr-ruEydoALgLHS2B4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:11+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" .
}