Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_assertion> ?p ?o ?g. }
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- NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_assertion type Assertion NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_head.
- NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_assertion description "[Fibrodysplasia ossificans progressiva (FOP; OMIM 135100) is a rare heritable disorder of connective tissue characterized by congenital malformations of the great toes and recurrent episodes of painful soft tissue swelling that lead to heterotopic ossifications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_provenance.
- NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_assertion evidence source_evidence_literature NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_provenance.
- NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_assertion SIO_000772 19300893 NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_provenance.
- NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_assertion wasDerivedFrom befree-20140225 NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_provenance.
- NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_assertion wasGeneratedBy ECO_0000203 NP415258.RARGf6jKWPBGhQdS2bSk-KKcZlkFUWC_mdmAz4IuAtXB4130_provenance.