Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance.
- NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_assertion description "[This includes cell lines derived from patients with relapsed disease featuring cytogenetic anomalies such as t(12;21), Philadelphia chromosome t(9;22), t(1;19) as well as a cell line carrying t(17;19) from a patient with de novo ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance.
- NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_assertion evidence source_evidence_literature NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance.
- NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_assertion SIO_000772 21960246 NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance.
- NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_assertion wasDerivedFrom befree-20150227 NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance.
- NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_assertion wasGeneratedBy ECO_0000203 NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP289209.RAYddKtsk_poMsiHHuOI91C3Crr31alD9EuEhAcNWLToE130_provenance.