@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM
> .
@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:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_head
{
this:
np:hasAssertion
dgn-np:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_assertion
;
np:hasProvenance
dgn-np:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_provenance
;
np:hasPublicationInfo
dgn-np:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_assertion
a
np:Assertion
.
dgn-np:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_provenance
a
np:Provenance
.
dgn-np:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_assertion
{
miriam-gene:3858
a
ncit:C16612
.
lld:C1843463
a
ncit:C7057
.
dgn-gda:DGN21c33f1e8c229387903ba3026cdd9edc
sio:SIO_000628
miriam-gene:3858
,
lld:C1843463
;
a
sio:SIO_001121
.
}
dgn-np:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_provenance
{
dgn-np:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_assertion
dcterms:description
"[Mutations within the rod domain, not in the beginning or the end of the rod domain, of keratin 10 were reported in annular epidermolytic ichthyosis (AEI), the distinct subtype of bullous congenital ichthyosiform erythroderma.]. 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:10511478
;
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:NP924808.RAFl_6zkJdLpEV8Zb2N0V_tz11hfRkcJ6KmfIa6w_d9kM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}