Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_assertion> ?p ?o ?g. }
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- NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_assertion type Assertion NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_head.
- NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_assertion description "[Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance.
- NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_assertion evidence source_evidence_literature NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance.
- NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_assertion SIO_000772 15472169 NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance.
- NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_assertion wasDerivedFrom befree-20150227 NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance.
- NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_assertion wasGeneratedBy ECO_0000203 NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance.