Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_assertion> ?p ?o ?g. }
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- NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_assertion type Assertion NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_head.
- NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_assertion description "[An autosomal dominant form of hereditary gingival fibromatosis (HGF, MIM 135300) was recently mapped to chromosome 2p21 in a large Brazilian family and there was an earlier report of GF in a boy with a cytogenetic duplication involving 2p13-->p21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_provenance.
- NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_assertion evidence source_evidence_literature NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_provenance.
- NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_assertion SIO_000772 10507724 NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_provenance.
- NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_assertion wasDerivedFrom befree-20140225 NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_provenance.
- NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_assertion wasGeneratedBy ECO_0000203 NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_provenance.