@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg
> .
@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:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_head
{
this:
np:hasAssertion
dgn-np:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_assertion
;
np:hasProvenance
dgn-np:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_provenance
;
np:hasPublicationInfo
dgn-np:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_assertion
a
np:Assertion
.
dgn-np:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_provenance
a
np:Provenance
.
dgn-np:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_assertion
{
miriam-gene:10683
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN294e010fed4d372c2d17c8a21b4b5ef0
sio:SIO_000628
miriam-gene:10683
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_provenance
{
dgn-np:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_assertion
dcterms:description
"[Although intact FHIT mRNA was detected as the main band in the remaining 37 samples, 33 of them (14 of 14 AML, 11 of 13 chronic myeloid leukemia, five of five acute lymphocytic leukemia, and three of five CLL) expressed aberrant FHIT delta 3-6 mRNA.]. 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:9170214
;
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:NP796953.RA4eeWWoTIzGSuALh1FVxM2Mhpb-IrrElSJHV2r6CecIg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}