Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP534687.RAFxA40tqminPQKah8PgzIZCmBSPGjaRLq03diluHmNMk130_provenance.