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- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion type Assertion NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_head.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion description "[TSP-5 is of interest because mutations in the gene cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED/EDM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion evidence source_evidence_literature NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion SIO_000772 18193163 NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion wasDerivedFrom befree-2016 NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion wasGeneratedBy ECO_0000203 NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.