@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4
> .
@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:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_head
{
this:
np:hasAssertion
dgn-np:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_assertion
;
np:hasProvenance
dgn-np:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_provenance
;
np:hasPublicationInfo
dgn-np:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_assertion
a
np:Assertion
.
dgn-np:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_provenance
a
np:Provenance
.
dgn-np:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_assertion
{
miriam-gene:10863
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGNa761406ed3ac08840db2b79403896e07
sio:SIO_000628
miriam-gene:10863
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_provenance
{
dgn-np:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_assertion
dcterms:description
"[The ADAM23 gene is frequently silenced in different types of tumors, and, in breast tumors, silencing is correlated with tumor progression, suggesting that it might be associated with the acquisition of a metastatic phenotype.]. 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:19549921
;
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:NP919833.RAgebpbkUusi8YeFhyq2TONSgzJ88PJV8oz_C10O_n0R4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:24+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" .
}