Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance.
- NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_assertion description "[Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance.
- NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_assertion evidence source_evidence_curated NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance.
- NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_assertion SIO_000772 12704386 NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance.
- NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_assertion wasDerivedFrom uniprot-20130724 NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance.
- NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_assertion wasGeneratedBy ECO_0000218 NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6603.RAoQFGhc8O5mZulaW36Mz2GBGAcpbv5kqzxKbQtfW1B28130_provenance.