Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance.
- NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_assertion wasGeneratedBy ECO_0000218 NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance.
- NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_assertion wasDerivedFrom uniprot-2016 NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance.
- NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_assertion SIO_000772 15140024 NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance.
- NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_assertion evidence source_evidence_curated NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance.
- NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_assertion description "[A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3443.RA3kkxO4BSBU8eDzKoK1jHnF2iRwuFuqK-DUueEo9-8VA130_provenance.