@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk
> .
@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:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_head
{
this:
np:hasAssertion
dgn-np:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_assertion
;
np:hasProvenance
dgn-np:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_provenance
;
np:hasPublicationInfo
dgn-np:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_assertion
a
np:Assertion
.
dgn-np:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_provenance
a
np:Provenance
.
dgn-np:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_assertion
{
miriam-gene:7070
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN6a7dea55fb3631aeb09d73c43c7f748a
sio:SIO_000628
miriam-gene:7070
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_provenance
{
dgn-np:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_assertion
dcterms:description
"[Sixteen patients with CML, six patients with AML, two patients with acute lymphatic leukemia (ALL) and one with chronic myelomonocytic leukemia (CMMOL), all with known cytogenetic abnormalities, were evaluated according to their CD90 (Thy-1)-positive or -negative phenotype.]. 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:10557051
;
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:NP378511.RAdfTUGDaggbCtxNKOhOGkuta6kq4e7WjVRkUdjvO-sYk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:41+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" .
}