@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs
> .
@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:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_head
{
this:
np:hasAssertion
dgn-np:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_assertion
;
np:hasProvenance
dgn-np:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_provenance
;
np:hasPublicationInfo
dgn-np:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_assertion
a
np:Assertion
.
dgn-np:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_provenance
a
np:Provenance
.
dgn-np:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0494165
a
ncit:C7057
.
dgn-gda:DGN4508c489ad777a9da5a1e139f5f6fd34
sio:SIO_000628
miriam-gene:3342
,
lld:C0494165
;
a
sio:SIO_001121
.
}
dgn-np:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_provenance
{
dgn-np:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_assertion
dcterms:description
"[We now report that Comparative Genomic Hybridization (CGH) and DNA PCR analyses of lung and liver metastases of human colon cancer show frequent gains in the region of chromosome 20q and have an increase in gene copy number of E2F-1.]. 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:14726656
;
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:NP876993.RATY4J3m9mfnMfL3z7fsFGQF7HL-ULFCDE2l1CErUOyfs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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" .
}