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- source_evidence_literature type ECO_0000212 NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_provenance.
- NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_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." NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_provenance.
- NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_assertion evidence source_evidence_literature NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_provenance.
- NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_assertion SIO_000772 15472169 NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_provenance.
- NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_assertion wasDerivedFrom befree-2016 NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_provenance.
- NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_assertion wasGeneratedBy ECO_0000203 NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_provenance.
- befree-2016 importedOn "2016-02-19" NP463547.RA3-7JrTDtON7Nn9tpviQN5MjFdJnjgW4OV3pQLKnb81k130_provenance.