@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y
> .
@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:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_head
{
this:
np:hasAssertion
dgn-np:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_assertion
;
np:hasProvenance
dgn-np:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_assertion
a
np:Assertion
.
dgn-np:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_provenance
a
np:Provenance
.
dgn-np:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_assertion
{
miriam-gene:55902
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN4c40db446aa8b53040d4de216444888b
sio:SIO_000628
miriam-gene:55902
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_provenance
{
dgn-np:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_assertion
dcterms:description
"[In order to determine whether adenoma-carcinoma sequence (ACS) or de novo cancer development, generally considered to be two separate genetic pathways, might be responsible, K-ras codon 12 mutations, good markers for ACS, were examined in 59 and 84 cases of advanced colorectal cancer surgically resected in Cancer Institute Hospital of the Japanese Foundation for Cancer Research in 1960-1969 and in 1990-1999, respectively.]. 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:15819719
;
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:NP684521.RAjVn_MIzWeOOcf-nDkXB0PUpBRWpQB-msr4Nixuz_A4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}