@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg
> .
@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:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_head
{
this:
np:hasAssertion
dgn-np:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_assertion
;
np:hasProvenance
dgn-np:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_provenance
;
np:hasPublicationInfo
dgn-np:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_assertion
a
np:Assertion
.
dgn-np:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_provenance
a
np:Provenance
.
dgn-np:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C0007758
a
ncit:C7057
.
dgn-gda:DGN25b09a8983159b335102faa981f536b2
sio:SIO_000628
miriam-gene:4854
,
lld:C0007758
;
a
sio:SIO_001121
.
}
dgn-np:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_provenance
{
dgn-np:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_assertion
dcterms:description
"[Besides their importance for the ongoing positional cloning of the CADASIL gene, these data help to refine the genetic mapping of CADASIL relative to familial hemiplegic migraine and hereditary paroxysmal cerebellar ataxia, conditions that we both mapped within the same chromosome 19 region.]. 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:8554054
;
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:NP894919.RAQ1XTVzG2pv7sWpeKJuUI5hvcu2QeL9V9U8wRmi0zigg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:10+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" .
}