@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc
> .
@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:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_head
{
this:
np:hasAssertion
dgn-np:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_assertion
;
np:hasProvenance
dgn-np:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_provenance
;
np:hasPublicationInfo
dgn-np:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_assertion
a
np:Assertion
.
dgn-np:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_provenance
a
np:Provenance
.
dgn-np:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_assertion
{
miriam-gene:54790
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNac9ee2b5594d770835828d6e03e5fa4f
sio:SIO_000628
miriam-gene:54790
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_provenance
{
dgn-np:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_assertion
dcterms:description
"[Furthermore cytogenetic studies are warranted in larger groups of MDS cases to identify newly acquired chromosome aberrations that may aid in cloning new genes involved in the neoplastic process, ultimately helping in the development of targeted therapeutic drugs.]. 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:21193364
;
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:NP913925.RAnGcHICpiwI3-a473yyj_aQRV1Uj8mMh91gDn0ow-oPc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:57+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" .
}