@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk
> .
@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:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_head
{
this:
np:hasAssertion
dgn-np:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_assertion
;
np:hasProvenance
dgn-np:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_assertion
a
np:Assertion
.
dgn-np:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_provenance
a
np:Provenance
.
dgn-np:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_assertion
{
miriam-gene:9112
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGNd123f18dc0305754c845248b3296dfc6
sio:SIO_000628
miriam-gene:9112
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_provenance
{
dgn-np:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_assertion
dcterms:description
"[Thus highly malignant cellular phenotypes can arise rapidly due to specific qualitative changes in critical controlling genes, or more slowly via less critical qualitative genetic changes coupled with other cellular changes, such as loss of intercellular communication, and changes in gene expression, such as in the MTA1 gene, resulting in cellular diversification and ultimately tumour progression to the metastatic state.]. 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:9513727
;
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:NP817558.RA3OQrlqERtiyeoe-xkMhy8BvcR8rNR1AOMSlu9VR0kFk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:21+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" .
}