@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk
> .
@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/v3.0.0/void/
> .
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_head
{
this:
np:hasAssertion
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_assertion
;
np:hasProvenance
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_provenance
;
np:hasPublicationInfo
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_assertion
a
np:Assertion
.
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_provenance
a
np:Provenance
.
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_assertion
{
miriam-gene:5111
a
ncit:C16612
.
lld:C0279626
a
ncit:C7057
.
dgn-gda:DGN1ec65ee15c13f2c29c21a76ee4348e78
sio:SIO_000628
miriam-gene:5111
,
lld:C0279626
;
a
sio:SIO_001121
.
}
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_provenance
{
dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_assertion
dcterms:description
"[The high coincident alterations for P53 and PCNA in SCC and GCA from the same patient indicate the possibility of similar molecular basis, which provides important molecular basis and etiological clue for similar geographic distribution and risk factors in SCC and GCA.]. 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:12508343
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:46+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: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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}