Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance.
- NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_assertion wasGeneratedBy ECO_0000203 NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance.
- NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_assertion wasDerivedFrom befree-2016 NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance.
- NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_assertion SIO_000772 9305598 NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance.
- NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_assertion evidence source_evidence_literature NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance.
- NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_assertion description "[Although deletion of ETV6 and t(12;21) were associated in most patients, in eight cases (six B lineage and two T-ALL) LOH was detected at the ETV6 locus without ETV6-AML1 hybrid RNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380849.RAl3mVBqd2iZyBse3T1XiPJu4C3pSA7XJiDr1H-DSiSDw130_provenance.