@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U
> .
@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:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_head
{
this:
np:hasAssertion
dgn-np:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_assertion
;
np:hasProvenance
dgn-np:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_provenance
;
np:hasPublicationInfo
dgn-np:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_assertion
a
np:Assertion
.
dgn-np:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_provenance
a
np:Provenance
.
dgn-np:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0494165
a
ncit:C7057
.
dgn-gda:DGNa7156f24988923ca0df396eb431ee405
sio:SIO_000628
miriam-gene:3342
,
lld:C0494165
;
a
sio:SIO_001121
.
}
dgn-np:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_provenance
{
dgn-np:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_assertion
dcterms:description
"[Comparative genomic hybridization (CGH) was used to screen for changes in the number of DNA sequence copies in 30 primary colorectal cancers and 16 liver metastases, to identify regions that contain genes important for the development and progression of colorectal cancer.]. 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:11745455
;
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:NP272299.RAbWQBdRfKoRRPcuY84EErdEPkGyTq0bvpOy6hhXOGx4U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:33+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" .
}