@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_head
{
this:
np:hasAssertion
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_assertion
;
np:hasProvenance
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_provenance
;
np:hasPublicationInfo
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_assertion
a
np:Assertion
.
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_provenance
a
np:Provenance
.
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN8608bbaf1cb5bfbcc48f0dd0ecea3168
sio:SIO_000628
miriam-gene:7157
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_provenance
{
dgn-np:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_assertion
dcterms:description
"[There were no other significant correlations with p53 point mutation or loss of heterozygosity in chromosomes 5q, 17p, and 18q and Rb gene, which have been suggested to be involved in the progression of CRC of both morphological types.]. 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:9699657
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1401540.RAe0k40514xt4pwdfjVviXfXJ3zocLp9Wk-NYfcZOB5NM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:21+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}