@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo
> .
@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:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_head
{
this:
np:hasAssertion
dgn-np:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_assertion
;
np:hasProvenance
dgn-np:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_provenance
;
np:hasPublicationInfo
dgn-np:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_assertion
a
np:Assertion
.
dgn-np:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_provenance
a
np:Provenance
.
dgn-np:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_assertion
{
miriam-gene:100
a
ncit:C16612
.
lld:C0406775
a
ncit:C7057
.
dgn-gda:DGN3f24c97c28dde4ec912a55d2042eaebe
sio:SIO_000628
miriam-gene:100
,
lld:C0406775
;
a
sio:SIO_001121
.
}
dgn-np:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_provenance
{
dgn-np:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_assertion
dcterms:description
"[Dyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant pigmentary genodermatosis characterized by hyperpigmented and hypopigmented macules of on the extremities and caused by the mutations in the ADAR gene(also called DSRAD) encoding for RNA-specific adenosine deaminase.]. 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:15146470
;
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:NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}