Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.
- NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.
- NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_assertion evidence source_evidence_literature NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.
- NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_assertion SIO_000772 18723471 NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.
- NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_assertion wasDerivedFrom gad-20150221 NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.
- NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_assertion wasGeneratedBy ECO_0000203 NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.