@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE
> .
@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:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_head
{
this:
np:hasAssertion
dgn-np:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_assertion
;
np:hasProvenance
dgn-np:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_provenance
;
np:hasPublicationInfo
dgn-np:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_assertion
a
np:Assertion
.
dgn-np:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_provenance
a
np:Provenance
.
dgn-np:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_assertion
{
miriam-gene:667
a
ncit:C16612
.
lld:C0014527
a
ncit:C7057
.
dgn-gda:DGNf21630095ee37de37da27b31546c25f0
sio:SIO_000628
miriam-gene:667
,
lld:C0014527
;
a
sio:SIO_001121
.
}
dgn-np:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_provenance
{
dgn-np:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_assertion
dcterms:description
"[We have also included new subtypes, such as autosomal dominant junctional EB and autosomal recessive EB due to mutations in the dystonin (DST) gene, which encodes the epithelial isoform of bullouspemphigoid antigen 1.]. 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:22137229
;
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:NP448762.RAqf7_T36Jav2GKrsilXyyOxUkx5lA_KHJkQDT8-p_TRE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:27+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" .
}