Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance.
- NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_assertion description "[CDKN2A mutations in Spanish cutaneous malignant melanoma families and patients with multiple melanomas and other neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance.
- NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_assertion evidence source_evidence_literature NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance.
- NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_assertion SIO_000772 10874641 NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance.
- NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_assertion wasDerivedFrom befree-2016 NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance.
- NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_assertion wasGeneratedBy ECO_0000203 NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance.
- befree-2016 importedOn "2016-02-19" NP287869.RAc7NPf7dFMnv4mQi6-ePdStFYI2XEhUlAEJyw_lMPgtA130_provenance.