Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance.
- NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_assertion description "[A p53 missense mutation was detected at codon 161 (GCC-->ACC, Ala-->Thr) in only one oligoastrocytoma without allelic loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance.
- NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_assertion evidence source_evidence_literature NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance.
- NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_assertion SIO_000772 12507133 NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance.
- NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_assertion wasDerivedFrom befree-20150227 NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance.
- NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_assertion wasGeneratedBy ECO_0000203 NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP830529.RAW3kRPOCLyONicdZk1GlEgB61ZayKiEwxrwAqudGxxQg130_provenance.