@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ
> .
@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:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_head
{
this:
np:hasAssertion
dgn-np:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_assertion
;
np:hasProvenance
dgn-np:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_assertion
a
np:Assertion
.
dgn-np:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_provenance
a
np:Provenance
.
dgn-np:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_assertion
{
miriam-gene:128408
a
ncit:C16612
.
lld:C0014527
a
ncit:C7057
.
dgn-gda:DGNef0cd627c0c65d2e87cb09b4d329308d
sio:SIO_000628
miriam-gene:128408
,
lld:C0014527
;
a
sio:SIO_001121
.
}
dgn-np:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_provenance
{
dgn-np:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_assertion
dcterms:description
"[We investigated the contribution of various segments of the beta4 integrin cytoplasmic domain in the formation of HDs in transient transfection studies using immortalized keratinocytes derived from an epidermolysis bullosa patient deficient in beta4 expression.]. 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:9660880
;
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:NP862357.RAg_WA8dENLXJAt-S5YIfnF1QMV-sn8sXWkA6FEIfvulQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:47+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
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"v2.1.0" .
}