@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o
> .
@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:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_head
{
this:
np:hasAssertion
dgn-np:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_assertion
;
np:hasProvenance
dgn-np:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_provenance
;
np:hasPublicationInfo
dgn-np:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_assertion
a
np:Assertion
.
dgn-np:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_provenance
a
np:Provenance
.
dgn-np:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_assertion
{
miriam-gene:10148
a
ncit:C16612
.
lld:C0033774
a
ncit:C7057
.
dgn-gda:DGNc513f75dfe3b858a47ba0be2c5e6bcac
sio:SIO_000628
miriam-gene:10148
,
lld:C0033774
;
a
sio:SIO_001121
.
}
dgn-np:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_provenance
{
dgn-np:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_assertion
dcterms:description
"[OSM and IL-31 signaling have been implicated in keratinocyte cell proliferation, differentiation, apoptosis, and inflammation, but our OSMR data in individuals with FPLCA represent the first human germline mutations in this cytokine receptor complex and provide new insight into mechanisms of skin itching.]. 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:18179886
;
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:NP915792.RAjhcN68tyj2gEYyiF-x3eWZAyjd5HDDmx48WxTpdGq3o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:22+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" .
}