Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance.
- NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_assertion description "[One pedigree was consistent with the Li-Fraumeni syndrome, and bone marrow from both diagnosis and remission indicated a germline G to T transversion at codon 272 (valine to leucine).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance.
- NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_assertion evidence source_evidence_curated NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance.
- NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_assertion SIO_000772 1737852 NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance.
- NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_assertion wasDerivedFrom uniprot-20130724 NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance.
- NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_assertion wasGeneratedBy ECO_0000218 NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6684.RAj4stqFGoqaUrQTb7sp2hu_ESNCnZIkJXArvebWKmeKc130_provenance.