@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs
> .
@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:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_head
{
this:
np:hasAssertion
dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_assertion
;
np:hasProvenance
dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_provenance
;
np:hasPublicationInfo
dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_assertion
a
np:Assertion
.
dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_provenance
a
np:Provenance
.
dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_assertion
{
miriam-gene:4519
a
ncit:C16612
.
lld:C0018203
a
ncit:C7057
.
dgn-gda:DGN01940752e1d7462c96db1a69e5e19884
sio:SIO_000628
miriam-gene:4519
,
lld:C0018203
;
a
sio:SIO_001121
.
}
dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_provenance
{
dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_assertion
dcterms:description
"[The diagnosis of CGD in both the latest male patient and the index male was confirmed by marked impairment in polymorphonuclear leucocyte oxidative burst activity in association with absence of both subunits of cytochrome b.]. 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:10844491
;
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:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}