@prefix dcterms: .
@prefix this: .
@prefix rdfs: .
@prefix xsd: .
@prefix sio: .
@prefix ncit: .
@prefix lld: .
@prefix miriam-gene: .
@prefix miriam-pubmed: .
@prefix eco: .
@prefix wi: .
@prefix prov: .
@prefix pav: .
@prefix prv: .
@prefix np: .
@prefix dgn-np: .
@prefix dgn-gda: .
@prefix dgn-void: .
dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_head {
this: np:hasAssertion dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_assertion;
np:hasProvenance dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_provenance;
np:hasPublicationInfo dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_publicationInfo;
a np:Nanopublication .
dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_assertion a np:Assertion .
dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_provenance a np:Provenance .
dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_publicationInfo a
np:PublicationInfo .
}
dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_assertion {
miriam-gene:2272 a ncit:C16612 .
lld:C1458155 a ncit:C7057 .
dgn-gda:DGN59ad1f3085ebbd3c208f4d78fbe0dde7 sio:SIO_000628 miriam-gene:2272, lld:C1458155;
a sio:SIO_001121 .
}
dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_provenance {
dgn-np:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_assertion dcterms:description
"[Analysis of 27 ovarian tumors demonstrating both loss and retention of 3p markers enabled us to define four nonoverlapping minimal deletion regions (OCLOHRs): (a) OCLOHR-1 mapped distal to D3S3591 at 3p25-26; (b) OCLOHR-2 mapped between D3S1317 and D3S1259 at 3p24-25; (c) OCLOHR-3 mapped between D3S1300 and D3S1284, an area that includes the FHIT locus at 3p14.2; and (d) OCLOHR-4 mapped between D3S1284 and D3S1274 at 3p12-13, a region known to contain overlapping homozygous deletions in lung and breast tumor cell lines.]. 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:10493522;
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:NP263598.RA1Rsj3rgdQakqMEHaBcvu6l0dKQFwMW-JEEMaV0xQZ4Q130_publicationInfo {
this: dcterms:created "2016-05-13T12:43:45+02:00"^^xsd:dateTime;
dcterms:rights ;
dcterms:rightsHolder dgn-void:IBIGroup;
dcterms:subject sio:SIO_000983;
prv:usedData dgn-void:disgenetv3.0rdf;
pav:authoredBy , ,
, , ;
pav:createdBy ;
pav:version "v4.0.0.0" .
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}