Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance.
- NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_assertion description "[The patient cohort was composed by 69 unrelated melanoma patients, 28 of whom were hereditary cases (with or without CDKN2A mutations) and 41 were isolated (sporadic) melanoma cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance.
- NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_assertion evidence source_evidence_literature NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance.
- NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_assertion SIO_000772 25647737 NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance.
- NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_assertion wasDerivedFrom befree-2016 NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance.
- NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_assertion wasGeneratedBy ECO_0000203 NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260713.RAozq4lOOB5ZrqFQXj5PFcpZ88s8xeVVmzddnd_jAPIos130_provenance.