@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8
> .
@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:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_head
{
this:
np:hasAssertion
dgn-np:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_assertion
;
np:hasProvenance
dgn-np:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_provenance
;
np:hasPublicationInfo
dgn-np:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_assertion
a
np:Assertion
.
dgn-np:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_provenance
a
np:Provenance
.
dgn-np:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN5253444d965346193580c4771ab945e6
sio:SIO_000628
miriam-gene:1029
,
lld:C0009324
;
a
sio:SIO_001121
.
}
dgn-np:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_provenance
{
dgn-np:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_assertion
dcterms:description
"[The low frequency of LOH in the p16 gene (9p) in adenomas compared with dysplasia in UC combined with infrequent LOH in APC gene loci in cases of pure dysplasia in UC may support this combination of markers as a clinical test for the differentiation of polypoid dysplasia from adenomas in UC.]. 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:9490271
;
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:NP923765.RA-9LbwlFZIkQZMgMBeiJo_kb7A_8npnKbKXtmvqBY9x8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}