@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg
> .
@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:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_head
{
this:
np:hasAssertion
dgn-np:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_assertion
;
np:hasProvenance
dgn-np:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_provenance
;
np:hasPublicationInfo
dgn-np:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_assertion
a
np:Assertion
.
dgn-np:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_provenance
a
np:Provenance
.
dgn-np:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_assertion
{
miriam-gene:4089
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN97e239a51da2e399cf82d0ed51ff82ec
sio:SIO_000628
miriam-gene:4089
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_provenance
{
dgn-np:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_assertion
dcterms:description
"[Five specific `malignant` events (gain of 8q, 13q, and 20q and loss of 17p and 18q) and aberrant staining for p53 and SMAD4 were all increased in the adenoma fractions of carcinoma cases compared with pure adenomas.]. 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:18245538
;
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:NP292824.RA9If572mYbpj8Zy4gdAuuGrhkmyD_2sgIWmGyLKewAYg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}