@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488
> .
@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:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_head
{
this:
np:hasAssertion
dgn-np:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_assertion
;
np:hasProvenance
dgn-np:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_provenance
;
np:hasPublicationInfo
dgn-np:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_assertion
a
np:Assertion
.
dgn-np:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_provenance
a
np:Provenance
.
dgn-np:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_assertion
{
miriam-gene:213
a
ncit:C16612
.
lld:C0026691
a
ncit:C7057
.
dgn-gda:DGN220a0b4bdb6440ad8b5a7c4a162f6132
sio:SIO_000628
miriam-gene:213
,
lld:C0026691
;
a
sio:SIO_001121
.
}
dgn-np:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_provenance
{
dgn-np:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_assertion
dcterms:description
"[Conclusively, incomplete KD, IVIG nonresponsiveness, long febrile days, and the rs7604693 genetic variant in the PELI1 gene are major risk factors for the development of CALs, whereas low serum albumin concentration is an independent risk factor for IVIG nonresponsiveness.]. 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:22105492
;
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:NP718570.RADmZqq6dBI4pc6EpzBxFbw6ARrAdU4fKv5-Iq8QDO488130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:16+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" .
}