Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_assertion> ?p ?o ?g. }
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- NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_assertion type Assertion NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_head.
- NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_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." NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.
- NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_assertion evidence source_evidence_literature NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.
- NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_assertion SIO_000772 10507724 NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.
- NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_assertion wasDerivedFrom befree-20140225 NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.
- NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_assertion wasGeneratedBy ECO_0000203 NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.