@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U
> .
@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:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_head
{
this:
np:hasAssertion
dgn-np:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_assertion
;
np:hasProvenance
dgn-np:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_provenance
;
np:hasPublicationInfo
dgn-np:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_assertion
a
np:Assertion
.
dgn-np:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_provenance
a
np:Provenance
.
dgn-np:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_assertion
{
miriam-gene:947
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNd9ca6d5ced7f6988472295ab3a87d19c
sio:SIO_000628
miriam-gene:947
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_provenance
{
dgn-np:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_assertion
dcterms:description
"[CD34+ bone marrow cells exhibit unique susceptibility to the development of specific chromosome aberrations that have been identified as the earliest structural changes occurring in the development of secondary myelodysplastic syndrome and acute myelogenous leukemia.]. 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:10706073
;
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:NP411501.RAu1nOmQ2esuB7ciLNStStuN-oAVtwJssANHSLUA48K1U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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" .
}