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- NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_assertion type Assertion NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_head.
- NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_assertion wasGeneratedBy ECO_0000203 NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_provenance.
- NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_assertion wasDerivedFrom befree-20150227 NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_provenance.
- NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_assertion SIO_000772 22050868 NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_provenance.
- NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_assertion evidence source_evidence_literature NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_provenance.
- NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_assertion description "[Patients with syndromic SCN were characterized for associated malformations and referred to us for G6PC3 mutational analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961868.RAA79A9df7ZswGfConyQT8T5ktv3uvnFR9BNc5P4GENh0130_provenance.