@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E
> .
@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:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_head
{
this:
np:hasAssertion
dgn-np:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_assertion
;
np:hasProvenance
dgn-np:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_provenance
;
np:hasPublicationInfo
dgn-np:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_assertion
a
np:Assertion
.
dgn-np:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_provenance
a
np:Provenance
.
dgn-np:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_assertion
{
miriam-gene:6774
a
ncit:C16612
.
lld:C0036439
a
ncit:C7057
.
dgn-gda:DGN007417986078e50213fd9218ff58b0e0
sio:SIO_000628
miriam-gene:6774
,
lld:C0036439
;
a
sio:SIO_001121
.
}
dgn-np:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_provenance
{
dgn-np:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_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-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:NP873992.RAyw_2acNJ2Is5ODpd7BE4uzVE8quvX3WV4MTmljNYj6E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}