Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance.
- NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_assertion description "[Among many gene alterations detected in human melanoma, defect of CDKN2A located at chromosome 9p21 seems to be most important in the earlier developmental phase, though significance of this gene in the evolution of melanoma in situ has not been confirmed yet.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance.
- NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_assertion evidence source_evidence_literature NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance.
- NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_assertion SIO_000772 11323215 NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance.
- NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_assertion wasDerivedFrom befree-20140225 NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance.
- NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_assertion wasGeneratedBy ECO_0000203 NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance.