@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A
> .
@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 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:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_head
{
this:
np:hasAssertion
dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_assertion
;
np:hasProvenance
dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_provenance
;
np:hasPublicationInfo
dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_assertion
a
np:Assertion
.
dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_provenance
a
np:Provenance
.
dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0027831
a
ncit:C7057
.
dgn-gda:DGNc7423db5b81cf7ded08ca201c4475509
sio:SIO_000628
miriam-gene:4360
,
lld:C0027831
;
a
sio:SIO_001121
.
}
dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_provenance
{
dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_assertion
dc:description
"[Nevertheless, the observation of frequent alterations of key growth regulatory genes in MMR-deficient cells such as NF1, APC, p53, K-Ras, with no significant excess of frameshift mutations and changes at short coding repeats, suggest that even in the presence of an inherited tendency to genomic instability, tumor progression is mainly driven by a process of natural selection.]. 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:16528606
;
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:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:44+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}