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- NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_assertion type Assertion NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_head.
- NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_provenance.
- NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_assertion evidence source_evidence_literature NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_provenance.
- NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_assertion SIO_000772 23712425 NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_provenance.
- NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_assertion wasDerivedFrom befree-20150227 NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_provenance.
- NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_assertion wasGeneratedBy ECO_0000203 NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_provenance.