Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance.
- NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_assertion description "[results reveal unique characteristics of BRCA1/2 mutation, genotype-phenotype & prognosis in moderate- & low-risk individuals of Greek ancestry; breast cancer due to mutations in BRCA1 & BRCA2 appears to be a heterogeneous syndrome in Greek population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance.
- NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_assertion evidence source_evidence_literature NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance.
- NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_assertion SIO_000772 15733268 NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance.
- NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_assertion wasDerivedFrom lhgdn-20090331 NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance.
- NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_assertion wasGeneratedBy ECO_0000203 NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP209450.RAD0DaGuhsWYu4FwJiPegkp3lR-_zhQV7oH0JbF4uAHZw130_provenance.