@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY
> .
@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:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_head
{
this:
np:hasAssertion
dgn-np:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_assertion
;
np:hasProvenance
dgn-np:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_provenance
;
np:hasPublicationInfo
dgn-np:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_assertion
a
np:Assertion
.
dgn-np:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_provenance
a
np:Provenance
.
dgn-np:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_assertion
{
miriam-gene:6422
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN44f7a9965e79ca1ae4d7931267ad4243
sio:SIO_000628
miriam-gene:6422
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_provenance
{
dgn-np:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_assertion
dcterms:description
"[Our results indicate that promoter hypermethylation is the predominant mechanism of SFRP1 gene silencing in human breast cancer and that SFRP1 gene inactivation in breast cancer is associated with unfavourable prognosis.]. 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:16449975
;
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:NP805015.RALcpW2zObWeyLKUaLyjEi3OGT8TBMF1nSskWX-GepJtY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:13+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" .
}