@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI
> .
@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:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_head
{
this:
np:hasAssertion
dgn-np:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_assertion
;
np:hasProvenance
dgn-np:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_provenance
;
np:hasPublicationInfo
dgn-np:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_assertion
a
np:Assertion
.
dgn-np:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_provenance
a
np:Provenance
.
dgn-np:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C1883018
a
ncit:C7057
.
dgn-gda:DGNb7753153fff821109eeaf2290d633ef9
sio:SIO_000628
miriam-gene:3918
,
lld:C1883018
;
a
sio:SIO_001121
.
}
dgn-np:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_provenance
{
dgn-np:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_assertion
dcterms:description
"[Additionally, no G-CSF receptor point mutations could be seen in neutrophils, blood and bone marrow mononuclear cells from patients with cyclic or idiopathic neutropenia, and bone marrow mononuclear cells from patients suffering from severe aplastic anemia.]. 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:9368331
;
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:NP579219.RAEX_-MGUnM_QsfTOhvKUOpkra7cClOxXMGrHY2u8EpHI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:49+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" .
}