@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE
> .
@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:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_head
{
this:
np:hasAssertion
dgn-np:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_assertion
;
np:hasProvenance
dgn-np:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_provenance
;
np:hasPublicationInfo
dgn-np:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_assertion
a
np:Assertion
.
dgn-np:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_provenance
a
np:Provenance
.
dgn-np:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_assertion
{
miriam-gene:2125
a
ncit:C16612
.
lld:C0546837
a
ncit:C7057
.
dgn-gda:DGNbc8472524a0af85d57ed1cfca7ae52b1
sio:SIO_000628
miriam-gene:2125
,
lld:C0546837
;
a
sio:SIO_001121
.
}
dgn-np:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_provenance
{
dgn-np:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_assertion
dcterms:description
"[The rate of EVPL gene mutation was quite low in contrast to the frequency of LOH on the TOC locus in sporadic OSCs, and the high incidence of oesophageal cancer development in tylosis families.]. 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:15756445
;
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:NP882938.RAdQ99I3FAzaynvrQ4YXgCVPT_dTFN9VeH1mNHT5OeMBE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}