Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.