Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_assertion> ?p ?o ?g. }
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- NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_assertion type Assertion NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_head.
- NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_assertion description "[epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_provenance.
- NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_assertion evidence source_evidence_literature NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_provenance.
- NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_assertion SIO_000772 11813134 NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_provenance.
- NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_assertion wasDerivedFrom lhgdn-20090331 NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_provenance.
- NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_assertion wasGeneratedBy ECO_0000203 NP193064.RAa56Qch2K7C7p0O768wFo23nA3oS-X5wdUabsQ7oVxL4130_provenance.