@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I
> .
@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:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_head
{
this:
np:hasAssertion
dgn-np:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_assertion
;
np:hasProvenance
dgn-np:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_provenance
;
np:hasPublicationInfo
dgn-np:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_assertion
a
np:Assertion
.
dgn-np:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_provenance
a
np:Provenance
.
dgn-np:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_assertion
{
miriam-gene:8091
a
ncit:C16612
.
lld:C0598935
a
ncit:C7057
.
dgn-gda:DGN7d220346e776c84abe4d0217da48c5b0
sio:SIO_000628
miriam-gene:8091
,
lld:C0598935
;
a
sio:SIO_001121
.
}
dgn-np:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_provenance
{
dgn-np:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_assertion
dcterms:description
"[Using positional cloning strategies, we and others previously identified HMGA1, HMGA2, RAD51L1, MORF, and, more recently, NCOA1 as primary target (fusion) genes associated with tumor initiation in four of these distinct cytogenetic subgroups.]. 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:22965931
;
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:NP600465.RAxV-SQW30dpuuSjTxLFDfqsblJTlta_ao-B8MnrnKw1I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}