@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc
> .
@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:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_head
{
this:
np:hasAssertion
dgn-np:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_assertion
;
np:hasProvenance
dgn-np:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_provenance
;
np:hasPublicationInfo
dgn-np:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_assertion
a
np:Assertion
.
dgn-np:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_provenance
a
np:Provenance
.
dgn-np:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1527408
a
ncit:C7057
.
dgn-gda:DGN551cdd56b40c0d2d0ddb0e75b31267ba
sio:SIO_000628
miriam-gene:7157
,
lld:C1527408
;
a
sio:SIO_001121
.
}
dgn-np:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_provenance
{
dgn-np:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_assertion
dcterms:description
"[Approximately half of all colorectal cancers show p53 (TP53) gene mutations, with higher frequencies observed in distal colon and rectal tumors and lower frequencies in proximal tumors and those with the microsatellite instability or methylator phenotypes.]. 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:12619112
;
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:NP456532.RAHYdYUawWwZDCiZSx729LE2uaXukGWwQY0ChfqSAtKTc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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" .
}