@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU
> .
@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:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_head
{
this:
np:hasAssertion
dgn-np:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_assertion
;
np:hasProvenance
dgn-np:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_provenance
;
np:hasPublicationInfo
dgn-np:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_assertion
a
np:Assertion
.
dgn-np:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_provenance
a
np:Provenance
.
dgn-np:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_assertion
{
miriam-gene:7037
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN163a12d258eaa6a778ee2803d9b56e70
sio:SIO_000628
miriam-gene:7037
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_provenance
{
dgn-np:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_assertion
dcterms:description
"[High resolution chromosomal analysis allowed us to define more precisely the chromosomal breakpoints to 3q26.2 and 21q22.2, close to the respective localizations of two genes important in cell proliferation and cancer pathogenesis: the transferrin receptor gene and the ets.2 proto-oncogene.]. 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:2747289
;
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:NP443872.RAyQkNzCFfZlaGYQ-yEoS8eqdSBRkdqmAj7w0q-jA2IvU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}