@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno
> .
@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:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_head
{
this:
np:hasAssertion
dgn-np:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_assertion
;
np:hasProvenance
dgn-np:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_provenance
;
np:hasPublicationInfo
dgn-np:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_assertion
a
np:Assertion
.
dgn-np:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_provenance
a
np:Provenance
.
dgn-np:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNd526da3143690436706511999b878568
sio:SIO_000628
miriam-gene:7157
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_provenance
{
dgn-np:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_assertion
dcterms:description
"[Twenty-six gastric carcinoma and matching normal tissue DNAs, which had previously been analyzed for alterations of the APC (adenomatous polyposis coli) and MCC (mutated in colorectal cancer) genes were further investigated for the following genetic alterations: mutation and loss of heterozygosity (LOH) of the p53 gene, replication error (RER) and LOH at 12 microsatellite repeat loci, and mutation of the hMSH2 gene.]. 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:11376803
;
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:NP159938.RAC91biY41Iu_gkmtNT69qBZcxswlRnN24ZuNvSVZzEno130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}