Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance.
- NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_assertion description "[To define the location and extent of deletions of 9p in NSCLC and MM, Southern blot analyses on six NSCLC and five MM cell lines using molecular probes to 9p loci (IFNA, IFNB1, D9S3, and D9S19) were performed, and DNA dosage was determined by densitometry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance.
- NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_assertion evidence source_evidence_literature NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance.
- NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_assertion SIO_000772 7688555 NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance.
- NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_assertion wasDerivedFrom befree-2016 NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance.
- NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_assertion wasGeneratedBy ECO_0000203 NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1318331.RAtafos0kQv9qhfwQse5naIXYXAsg_hanX0kMVyiOH6-8130_provenance.