Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance.
- NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_assertion wasGeneratedBy ECO_0000203 NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance.
- NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_assertion wasDerivedFrom befree-20150227 NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance.
- NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_assertion SIO_000772 15374878 NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance.
- NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_assertion evidence source_evidence_literature NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance.
- NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_assertion description "[Cases of ALL with MLL gene rearrangements and those with high hyperdiploidy (> 50 chromosomes) express the highest levels of FLT3, and activating mutations of FLT3 occur in 18% of MLL-rearranged and 28% of hyperdiploid ALL cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559405.RAlN35vOSiZtHDlGYzhE436VtlKExzQS-ZF_g7dSbbTzE130_provenance.