Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_assertion> ?p ?o ?g. }
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- NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_assertion type Assertion NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_head.
- NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_assertion description "[The majority of the somatic mutations identified were identical to germline activating mutations in FGFR2 and FGFR3 that cause Apert Syndrome, Beare-Stevenson Syndrome, hypochondroplasia, achondroplasia and SADDAN syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_provenance.
- NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_assertion evidence source_evidence_literature NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_provenance.
- NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_assertion SIO_000772 17525745 NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_provenance.
- NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_assertion wasDerivedFrom befree-20140225 NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_provenance.
- NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_assertion wasGeneratedBy ECO_0000203 NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_provenance.