@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI
> .
@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:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_head
{
this:
np:hasAssertion
dgn-np:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_assertion
;
np:hasProvenance
dgn-np:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_provenance
;
np:hasPublicationInfo
dgn-np:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_assertion
a
np:Assertion
.
dgn-np:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_provenance
a
np:Provenance
.
dgn-np:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_assertion
{
miriam-gene:5339
a
ncit:C16612
.
lld:C0079298
a
ncit:C7057
.
dgn-gda:DGN35a73ba0d371dbedecdcf035659ac7b7
sio:SIO_000628
miriam-gene:5339
,
lld:C0079298
;
a
sio:SIO_001121
.
}
dgn-np:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_provenance
{
dgn-np:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_assertion
dcterms:description
"[Consistent with the absence of muscular symptoms in these patients, muscle biopsies from several epidermolysis bullosa simplex Ogna members of the Norwegian kindred showed normal staining patterns using antibodies to plectin.]. 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:11851880
;
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:NP486958.RAbp0N_H_A8JZmAJ8m8LHhIh4Qg6Y8KbxqI-7ZY4NlSLI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}