Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion type Assertion NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_head.
- NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion wasGeneratedBy ECO_0000203 NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_provenance.
- NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion wasDerivedFrom befree-20140225 NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_provenance.
- NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion SIO_000772 22619094 NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_provenance.
- NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion evidence source_evidence_literature NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_provenance.
- NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion description "[These findings indicate that the distribution of NOTCH1 mutations in CLL with trisomy 12 is heterogeneous and that the presence of additional chromosomal abnormalities such as trisomy 18 could change the prognosis of these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_provenance.