@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g
> .
@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/v4.0.0/void/
> .
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_head
{
this:
np:hasAssertion
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_assertion
;
np:hasProvenance
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_assertion
a
np:Assertion
.
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_provenance
a
np:Provenance
.
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_assertion
{
miriam-gene:1441
a
ncit:C16612
.
lld:C0023481
a
ncit:C7057
.
dgn-gda:DGN81ed0dd9bcc94ae52b16590774f44efd
sio:SIO_000628
miriam-gene:1441
,
lld:C0023481
;
a
sio:SIO_001121
.
}
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_provenance
{
dgn-np:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_assertion
dcterms:description
"[The diagnosis of CNL will no longer be one only of exclusion, and revision of the current WHO diagnostic criteria is expected to include the molecular criterion of CSF3R mutation positivity.]. 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:24335708
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1136500.RAtM2-Ff9eAKCb1oY8GMiJKyKpN0-AnilWbkb4zlHnk4g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:21+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}