Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_assertion> ?p ?o ?g. }
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- NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_assertion type Assertion NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_head.
- NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_assertion wasGeneratedBy ECO_0000203 NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_provenance.
- NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_assertion wasDerivedFrom befree-20140225 NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_provenance.
- NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_assertion SIO_000772 23532954 NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_provenance.
- NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_assertion evidence source_evidence_literature NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_provenance.
- NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_assertion description "[Pfeiffer syndrome is an autosomal dominant condition classically combining craniosynostosis with digital anomalies of the hands and feet.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705815.RAQhWmzoscrFYDknnqRGaUKABI2ru7vYgh3opr_O_ScOo130_provenance.