@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg
> .
@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:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_head
{
this:
np:hasAssertion
dgn-np:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_assertion
;
np:hasProvenance
dgn-np:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_provenance
;
np:hasPublicationInfo
dgn-np:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_assertion
a
np:Assertion
.
dgn-np:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_provenance
a
np:Provenance
.
dgn-np:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN463b9b9d446af9cef99db8e14fd1f131
sio:SIO_000628
miriam-gene:861
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_provenance
{
dgn-np:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_assertion
dcterms:description
"[For example, the TEL-AML1 fusion, the most common genetic abnormality in childhood acute lymphoblastic leukemia, was recently shown to be an independent, favorable prognostic factor, suggesting that patients with this abnormality are best treated with conventional antimetabolite-based therapy.]. 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:9260050
;
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:NP257106.RAUI-eSCmeeQZM_Yc6S6zRec23miWgvqXVYEU83E8gXVg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}