@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ
> .
@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:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_head
{
this:
np:hasAssertion
dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_assertion
;
np:hasProvenance
dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_assertion
a
np:Assertion
.
dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_provenance
a
np:Provenance
.
dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_assertion
{
miriam-gene:5530
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGNa073612622d5e1629d80136c59d1a188
sio:SIO_000628
miriam-gene:5530
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_provenance
{
dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_assertion
dcterms:description
"[Although chromosomal structural anomaly is presumed to play an important role in the carcinogenesis of CRC, chromosomal copy number alterations (CNA) and loss of heterozygosity (LOH) have not yet been analyzed extensively at high resolution in CRC.]. 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:18564138
;
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:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:09+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" .
}