Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_assertion type Assertion NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_head.
- NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_assertion description "[Missense variants of the ATM gene are a rare event in childhood Hodgkin disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_provenance.
- NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_assertion evidence source_evidence_literature NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_provenance.
- NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_assertion SIO_000772 14735203 NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_provenance.
- NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_assertion wasDerivedFrom befree-20140225 NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_provenance.
- NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_assertion wasGeneratedBy ECO_0000203 NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_provenance.