@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps
> .
@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:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_head
{
this:
np:hasAssertion
dgn-np:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_assertion
;
np:hasProvenance
dgn-np:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_provenance
;
np:hasPublicationInfo
dgn-np:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_assertion
a
np:Assertion
.
dgn-np:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_provenance
a
np:Provenance
.
dgn-np:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_assertion
{
miriam-gene:3858
a
ncit:C16612
.
lld:C0079298
a
ncit:C7057
.
dgn-gda:DGNf9cb34d897b5c1c7530ba6bd10059a7d
sio:SIO_000628
miriam-gene:3858
,
lld:C0079298
;
a
sio:SIO_001121
.
}
dgn-np:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_provenance
{
dgn-np:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_assertion
dcterms:description
"[Keratin disorders are a novel molecular category including quite different phenotypes such as epidermolysis bullosa simplex (EBS), bullous congenital ichthyosiform erthroderma (BCIE), pachyonychia congenital (PC), steatocystoma multiplex, ichthyosis bullosa of Siemens (IBS), and white sponge nevus (WSN) of the orogenital mucosa.]. 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:15452838
;
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:NP654969.RAoQV_tj_6BwrNURg_w64EGhblJCzOwaAoiHqKwLa0fps130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:34+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" .
}