@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k
> .
@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:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_head
{
this:
np:hasAssertion
dgn-np:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_assertion
;
np:hasProvenance
dgn-np:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_provenance
;
np:hasPublicationInfo
dgn-np:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_assertion
a
np:Assertion
.
dgn-np:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_provenance
a
np:Provenance
.
dgn-np:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_assertion
{
miriam-gene:6774
a
ncit:C16612
.
lld:C0340613
a
ncit:C7057
.
dgn-gda:DGNf0bb0373788dc8d38becd8606e9148bf
sio:SIO_000628
miriam-gene:6774
,
lld:C0340613
;
a
sio:SIO_001121
.
}
dgn-np:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_provenance
{
dgn-np:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_assertion
dcterms:description
"[In depth study of the role of STAT3 mutations in specific aspects of HIES may lead to better understanding and new approaches to treatment of conditions intrinsic to HIES that are common in the general population, such as staphylococcal infections, scoliosis, osteoporosis, bronchiectasis, and arterial aneurysms.]. 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:19452285
;
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:NP739836.RAfDeL0nYH51m-eSr3sIikiMHu2wmm13oZjGb87Zaz88k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:20+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" .
}