Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_assertion> ?p ?o ?g. }
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- NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_assertion type Assertion NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_head.
- NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_assertion description "[Mutation detection rates were highest in those with a positive family history (62%), malignancy (53%), multiple tumours (33%) or PGL (44%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_provenance.
- NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_assertion evidence source_evidence_literature NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_provenance.
- NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_assertion SIO_000772 23072324 NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_provenance.
- NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_assertion wasDerivedFrom befree-2016 NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_provenance.
- NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_assertion wasGeneratedBy ECO_0000203 NP1021603.RAObvuXMt66nAMfw0pSP3ZBBjI9d-54WAdwA7CgolNqr0130_provenance.