@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg
> .
@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:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_head
{
this:
np:hasAssertion
dgn-np:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_assertion
;
np:hasProvenance
dgn-np:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_provenance
;
np:hasPublicationInfo
dgn-np:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_assertion
a
np:Assertion
.
dgn-np:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_provenance
a
np:Provenance
.
dgn-np:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_assertion
{
miriam-gene:6663
a
ncit:C16612
.
lld:C0019569
a
ncit:C7057
.
dgn-gda:DGNb51711c8507479b3d04769b253e77d48
sio:SIO_000628
miriam-gene:6663
,
lld:C0019569
;
a
sio:SIO_001121
.
}
dgn-np:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_provenance
{
dgn-np:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_assertion
dcterms:description
"[To understand the molecular basis for the pathogenesis of HD we intended to determine the specific cell lineages in the enteric nervous system which normally express SOX10 but are affected in disease conditions.]. 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:11454798
;
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:NP439937.RA_goXpwLm2x9GgFwhG_P83voTjBAeBdGtT0mnbZm6KNg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}