Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_assertion type Assertion NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_head.
- NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_assertion wasGeneratedBy ECO_0000203 NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_provenance.
- NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_assertion wasDerivedFrom befree-2016 NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_provenance.
- NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_assertion SIO_000772 21533187 NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_provenance.
- NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_assertion evidence source_evidence_literature NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_provenance.
- NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_assertion description "[MC is clinically distinct from other multiple exostosis or multiple enchondromatosis syndromes and is unlinked to EXT1 and EXT2, the genes responsible for autosomal dominant multiple osteochondromas (MO).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890800.RAdHHVQuV70qkbtTFYgD53FILJP8qbdbJKg-_PI6ogGsQ130_provenance.