@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M
> .
@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:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_head
{
this:
np:hasAssertion
dgn-np:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_assertion
;
np:hasProvenance
dgn-np:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_provenance
;
np:hasPublicationInfo
dgn-np:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_assertion
a
np:Assertion
.
dgn-np:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_provenance
a
np:Provenance
.
dgn-np:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN3211dc6fed943479f42e7ba9dfe2e093
sio:SIO_000628
miriam-gene:324
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_provenance
{
dgn-np:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_assertion
dcterms:description
"[Since the occurrence of an APC mutation is considered an early event in colorectal carcinogenesis, our findings indicating an extremely low frequency of such changes in and around the MCR suggest that carcinomas of the small intestine arise via a genetic pathway distinct from that involved in the development of carcinomas of the colorectum.]. 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:9033644
;
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:NP218233.RAYjl4RBmGClCJwZSKOq-UfhSUpHjQkH0Sq5Zja0_ql5M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+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" .
}