@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y
> .
@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:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_head
{
this:
np:hasAssertion
dgn-np:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_assertion
;
np:hasProvenance
dgn-np:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_assertion
a
np:Assertion
.
dgn-np:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_provenance
a
np:Provenance
.
dgn-np:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_assertion
{
miriam-gene:6774
a
ncit:C16612
.
lld:C0038160
a
ncit:C7057
.
dgn-gda:DGN62ab9f7a9ab4159d1d140b6f5733b4e7
sio:SIO_000628
miriam-gene:6774
,
lld:C0038160
;
a
sio:SIO_001121
.
}
dgn-np:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_provenance
{
dgn-np:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_assertion
dcterms:description
"[Further understanding of how STAT3 results in the diverse manifestations of HIES will allow us to develop more specific therapies for HIES as well as for many of the manifestations, such as scoliosis, recurrent staphylococcal infections, and eczema, which are common in the general population.]. 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:19190525
;
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:NP433877.RAfqVqc_-uWWPfB2eTq01Y0qVMm7tfD15GI-4MzHsxo1Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:17+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" .
}