@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_head
{
this:
np:hasAssertion
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_assertion
;
np:hasProvenance
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_provenance
;
np:hasPublicationInfo
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_assertion
a
np:Assertion
.
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_provenance
a
np:Provenance
.
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_assertion
{
miriam-gene:1991
a
ncit:C16612
.
lld:C0023530
a
ncit:C7057
.
dgn-gda:DGNa817be713ccd908410fd41516210205b
sio:SIO_000628
miriam-gene:1991
,
lld:C0023530
;
a
sio:SIO_001122
.
}
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_provenance
{
dgn-np:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_assertion
dcterms:description
"[These observations provide further insight into potential mechanisms by which NE mutations cause neutropenia and suggest that abnormal protein trafficking and accelerated apoptosis of differentiating myeloid cells contribute to the severe SCN phenotype resulting from the G185R mutation.]. 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:15657182
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP372721.RAPm8EolbLtpS7yKoQwj4boQrPq2DD_7J6tOqQHCyPBwI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:15+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}