Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance.
- NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_assertion description "[Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance.
- NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_assertion evidence source_evidence_curated NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance.
- NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_assertion SIO_000772 13680526 NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance.
- NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_assertion wasDerivedFrom uniprot-20130724 NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance.
- NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_assertion wasGeneratedBy ECO_0000218 NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP169.RA4raXNULahaN5QJTxsHVQ7_XI0qXtLYxCcHq5R45l768130_provenance.