Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance.
- NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_assertion description "[Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance.
- NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_assertion evidence source_evidence_curated NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance.
- NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_assertion SIO_000772 9207788 NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance.
- NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_assertion wasDerivedFrom ctd_human-2016 NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance.
- NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_assertion wasGeneratedBy ECO_0000218 NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP37522.RAknkzyXohRNLdvYzP3UuquSu6flfHEzVol65ScdBc5Aw130_provenance.