@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs
> .
@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:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_head
{
this:
np:hasAssertion
dgn-np:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_assertion
;
np:hasProvenance
dgn-np:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_provenance
;
np:hasPublicationInfo
dgn-np:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_assertion
a
np:Assertion
.
dgn-np:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_provenance
a
np:Provenance
.
dgn-np:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_assertion
{
miriam-gene:5266
a
ncit:C16612
.
lld:C0152081
a
ncit:C7057
.
dgn-gda:DGNfb431f7dcfb621163e7631d6e65f60ed
sio:SIO_000628
miriam-gene:5266
,
lld:C0152081
;
a
sio:SIO_001121
.
}
dgn-np:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_provenance
{
dgn-np:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_assertion
dcterms:description
"[Our data indicate that the decrease in SKALP activity in pustular psoriasis is not caused by mutations in the coding region of the gene, and that there is no allelic association between pustular psoriasis and SKALP gene polymorphisms.]. 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:9727750
;
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:NP905325.RAheCOAduKus3uIZ1i4-scezw6VV6Vh0yCKWNgxaRaHRs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:16+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" .
}