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http://rdf.disgenet.org/nanopublications.trig#NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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:NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs130_head
{
this:
np:hasAssertion
dgn-np:NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs130_assertion
a
np:Assertion
.
dgn-np:NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs130_provenance
a
np:Provenance
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dgn-np:NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs130_publicationInfo
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np:PublicationInfo
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}
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{
miriam-gene:805
a
ncit:C16612
.
lld:C0037772
a
ncit:C7057
.
dgn-gda:DGNe83cfd368fb4c2a2f60eace3193a35c9
sio:SIO_000628
miriam-gene:805
,
lld:C0037772
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.
}
dgn-np:NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs130_provenance
{
dgn-np:NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs130_assertion
dcterms:description
"[The suggestion that the three X linked syndromes X linked spastic paraplegia (MIM 312900), MASA syndrome (MIM 303350), and X linked hydrocephalus owing to stenosis of the aqueduct of Sylvius (MIM 307000) are variable clinical manifestations of mutations at the same locus at Xq28 was confirmed by the finding of mutations in the L1-CAM gene in the three syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:7562969
;
prov:wasDerivedFrom
dgn-void:befree-20140225
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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 .
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dgn-np:NP475885.RAEQNzEkH3w6yShGcVlfERlYCjjeeQlJ9IdiC426KPsDs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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
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<
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> , <
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> , <
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> ;
pav:createdBy
<
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}