Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion> ?p ?o ?g. }
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- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion type Assertion NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_head.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion description "[NOTCH1 mutations, found in 63 patients (11%), were associated with unmutated IGHV, high expression of CD38 and ZAP-70, trisomy 12, advanced stage and elevated lactate dehydrogenase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion evidence source_evidence_literature NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion SIO_000772 23295735 NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion wasDerivedFrom befree-20140225 NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion wasGeneratedBy ECO_0000203 NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.