@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA
> .
@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:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_head
{
this:
np:hasAssertion
dgn-np:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_assertion
;
np:hasProvenance
dgn-np:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_provenance
;
np:hasPublicationInfo
dgn-np:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_assertion
a
np:Assertion
.
dgn-np:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_provenance
a
np:Provenance
.
dgn-np:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_assertion
{
miriam-gene:7019
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNa33370583fbe0a48e6e5d95008fe208d
sio:SIO_000628
miriam-gene:7019
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_provenance
{
dgn-np:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_assertion
dcterms:description
"[Here, we report the identification of frequent frameshift mutations in the coding mononucleotide repeat of TFAM in sporadic colorectal cancer (CRC) cell lines and in primary tumors with microsatellite instability (MSI), but not in microsatellite stable (MSS) CRC cell lines and tumors.]. 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:21467167
;
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:NP385408.RAw9Vi5t6I-que5s45BaXQkdkasgTXqkr-vbcOHqOXdAA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:49+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" .
}