@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_head
{
this:
np:hasAssertion
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_assertion
;
np:hasProvenance
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_provenance
;
np:hasPublicationInfo
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_assertion
a
np:Assertion
.
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_provenance
a
np:Provenance
.
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_assertion
{
miriam-gene:1630
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGN98f8c822e71c6266914b88de48d47593
sio:SIO_000628
miriam-gene:1630
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_provenance
{
dgn-np:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_assertion
dcterms:description
"[Thus, we propose that the frequent allelic loss at 18q is because of the effect of multiple genes, and there is at least one as yet unidentified tumor suppressor gene at 18q residing distal to SMAD4, SMAD2, and DCC involved in serous ovarian carcinoma.]. 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:11438451
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP322818.RApxeGQgh_gBnRLmLLma8gEuTjUzZ_wwlpQpWxHRT1Zik130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:11+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}