@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_head
{
this:
np:hasAssertion
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_assertion
;
np:hasProvenance
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_provenance
;
np:hasPublicationInfo
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_assertion
a
np:Assertion
.
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_provenance
a
np:Provenance
.
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_assertion
{
miriam-gene:2312
a
ncit:C16612
.
lld:C0474892
a
ncit:C7057
.
dgn-gda:DGN76e7beaa4613ae3f5d5178e1a86842e3
sio:SIO_000628
miriam-gene:2312
,
lld:C0474892
;
a
sio:SIO_001121
.
}
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_provenance
{
dgn-np:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_assertion
dcterms:description
"[Mutations in the filament aggregating protein (filaggrin) gene have recently been identified as the cause of the common genetic skin disorder ichthyosis vulgaris (IV), the most prevalent inherited disorder of keratinization.]. 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:16810297
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP557422.RAeBzM-oTIyu0QMRPWNUsxvtYO7x8ILVFOmP8cAYOxFw4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:57+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}