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- NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_assertion type Assertion NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_head.
- NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_assertion description "[FGFR3 germline mutations cause autosomal dominant skeletal disorders including achondroplasia, thanatophoric dysplasia, severe achondroplasia with developmental delay and acanthosis nigricans, and Crouzon syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_provenance.
- NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_assertion evidence source_evidence_literature NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_provenance.
- NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_assertion SIO_000772 16778799 NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_provenance.
- NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_assertion wasDerivedFrom befree-2016 NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_provenance.
- NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_assertion wasGeneratedBy ECO_0000203 NP555206.RAd2vWuBsWWAGServ68keIPVfjsRU3wtKVt5gBtSZany0130_provenance.