@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E
> .
@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:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_head
{
this:
np:hasAssertion
dgn-np:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_assertion
;
np:hasProvenance
dgn-np:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_provenance
;
np:hasPublicationInfo
dgn-np:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_assertion
a
np:Assertion
.
dgn-np:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_provenance
a
np:Provenance
.
dgn-np:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0086692
a
ncit:C7057
.
dgn-gda:DGNe85fc56a24d7f2711ee8e37d609d2c5f
sio:SIO_000628
miriam-gene:7248
,
lld:C0086692
;
a
sio:SIO_001121
.
}
dgn-np:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_provenance
{
dgn-np:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_assertion
dcterms:description
"[We have studied 146 ovarian tumours (94 carcinomas, 22 tumours of low malignant potential and 30 benign tumours) for evidence of allele loss on chromosome 17p and 17q sufficient to imply the proximity of a tumour-suppressor gene.]. 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:1408149
;
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:NP796655.RApd7nPr4cvAA7kyIo3lcGdzGhuwROPmxcTIxe4dNUT_E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}