Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance.
- NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_assertion description "[Human adenylosuccinate lyase (ADSL), cloning and characterization of full-length cDNA and its isoform, gene structure and molecular basis for ADSL deficiency in six patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance.
- NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_assertion evidence source_evidence_curated NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance.
- NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_assertion SIO_000772 10888601 NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance.
- NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_assertion wasDerivedFrom ctd_human-20150221 NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance.
- NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_assertion wasGeneratedBy ECO_0000218 NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP6071.RAU6Hm2uKCXNM6MlINgUNwwELjwNaSnUMoGunDVVtf-VA130_provenance.