Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance.
- NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_assertion wasGeneratedBy ECO_0000203 NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance.
- NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_assertion wasDerivedFrom befree-20150227 NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance.
- NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_assertion SIO_000772 23082473 NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance.
- NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_assertion evidence source_evidence_literature NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance.
- NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_assertion description "[Chromosomal aberrations were found to be present in 76.6% of our patients with 13q deletion as the most frequent abnormality in our patients (46.7%), followed by trisomy 12 (36.7%), then ATM and p53 deletion (26.7%) each.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255597.RAQ91RM-JEWszT0ge4XWDY2Aq7D1zLlpBHB-YL5u1o__M130_provenance.