@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I
> .
@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:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_head
{
this:
np:hasAssertion
dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_assertion
;
np:hasProvenance
dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_provenance
;
np:hasPublicationInfo
dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_assertion
a
np:Assertion
.
dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_provenance
a
np:Provenance
.
dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0153381
a
ncit:C7057
.
dgn-gda:DGNc54e0e98a2fa0c32d025303d8b91fa78
sio:SIO_000628
miriam-gene:324
,
lld:C0153381
;
a
sio:SIO_001121
.
}
dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_provenance
{
dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_assertion
dcterms:description
"[Because of similar causes of oral and esophageal cancers, we investigated allelic deletion of the adenomatous polyposis coli gene in oral cancers by examining tumor cells of persons normally heterozygous at a polymorphic restriction site in adenomatous polyposis coli.]. 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:8170656
;
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:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}