@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so
> .
@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:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_head
{
this:
np:hasAssertion
dgn-np:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_assertion
;
np:hasProvenance
dgn-np:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_provenance
;
np:hasPublicationInfo
dgn-np:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_assertion
a
np:Assertion
.
dgn-np:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_provenance
a
np:Provenance
.
dgn-np:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_assertion
{
miriam-gene:3858
a
ncit:C16612
.
lld:C0020758
a
ncit:C7057
.
dgn-gda:DGN8cc3da89ced2a5d37b0b2153b196629e
sio:SIO_000628
miriam-gene:3858
,
lld:C0020758
;
a
sio:SIO_001121
.
}
dgn-np:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_provenance
{
dgn-np:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_assertion
dcterms:description
"[A type of lamellar ichthyosis may be explained on the basis of abnormal cornified cell envelope formation, and bullous congenital ichthyosiform erythroderma (epidermolytic hyperkeratosis) is caused by mutations in keratins K1 or K10.]. 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:7951667
;
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:NP642505.RAg_FTvVeN6mbiqtVussk-QmXWiLiMB9iB5qHibeLX2so130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:27+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" .
}