@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE
> .
@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:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_head
{
this:
np:hasAssertion
dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_assertion
;
np:hasProvenance
dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_provenance
;
np:hasPublicationInfo
dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_assertion
a
np:Assertion
.
dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_provenance
a
np:Provenance
.
dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_assertion
{
miriam-gene:9555
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN53a3b61e2ad610c584188bd874822f9f
sio:SIO_000628
miriam-gene:9555
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_provenance
{
dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_assertion
dcterms:description
"[These results show the power of combined array CGH and SAGE analysis for the identification of candidate amplicon targets and identify H2AFJ and EPS8 as novel putative oncogenes in breast cancer.]. 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:16618726
;
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:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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" .
}