Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance.
- befree-2016 importedOn "2016-02-19" NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance.
- NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_assertion wasGeneratedBy ECO_0000203 NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance.
- NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_assertion wasDerivedFrom befree-2016 NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance.
- NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_assertion SIO_000772 20032395 NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance.
- NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_assertion evidence source_evidence_literature NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance.
- NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_assertion description "[Numerical aberrations of chromosome 9 and p16 gene deletion are common findings in all subtypes of non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783406.RAipLbBmFoDK-bZzfusv_E900VMkXjJySsFOo8MLucPZA130_provenance.