@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM
> .
@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:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_head
{
this:
np:hasAssertion
dgn-np:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_assertion
;
np:hasProvenance
dgn-np:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_provenance
;
np:hasPublicationInfo
dgn-np:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_assertion
a
np:Assertion
.
dgn-np:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_provenance
a
np:Provenance
.
dgn-np:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_assertion
{
miriam-gene:10007
a
ncit:C16612
.
lld:C0031106
a
ncit:C7057
.
dgn-gda:DGNe5b4eed90d3e70daf71aad500c2ac769
sio:SIO_000628
miriam-gene:10007
,
lld:C0031106
;
a
sio:SIO_001121
.
}
dgn-np:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_provenance
{
dgn-np:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_assertion
dcterms:description
"[GPI anchors of CD16 on neutrophils from controls and patients were both partially resistant to phosphatidylinositol-specific phospholipase C. The presence of promyelocytes in peripheral blood, low expression of CD16, and low chemotactic response of neutrophils suggest that patients with EOP have an abnormal maturation system in myeloid lineage cells in the bone marrow, which may be associated with the onset and course of EOP.]. 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:9284170
;
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:NP691805.RAJUadQr0_Dtk7wq4XqUU7fGJlWe800q7Q-DAjx6sbHmM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}