@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg
> .
@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:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_head
{
this:
np:hasAssertion
dgn-np:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_assertion
;
np:hasProvenance
dgn-np:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_provenance
;
np:hasPublicationInfo
dgn-np:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_assertion
a
np:Assertion
.
dgn-np:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_provenance
a
np:Provenance
.
dgn-np:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0007130
a
ncit:C7057
.
dgn-gda:DGNdbf9ecd4a49c267ea89d771e67e9185a
sio:SIO_000628
miriam-gene:324
,
lld:C0007130
;
a
sio:SIO_001121
.
}
dgn-np:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_provenance
{
dgn-np:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_assertion
dcterms:description
"[Inactivation of other tumor suppressor genes by mutation (APC, p16) or hypermethylation (p16) as well as amplification of oncogenes such as cerbB2 are relatively late events in the development of adenocarcinoma.]. 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:10212817
;
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:NP413535.RAM_S8Zr7J6uwWcbMMLh4j54etoRo_sZjNajlYBSLVgqg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}