Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance.
- NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_assertion description "[Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance.
- NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_assertion evidence source_evidence_curated NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance.
- NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_assertion SIO_000772 10973259 NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance.
- NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_assertion wasDerivedFrom uniprot-2016 NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance.
- NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_assertion wasGeneratedBy ECO_0000218 NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP997.RAj2QzcTF0yq9-qARF4vrxg30lrw8ZteAB_kdaVa_hwVQ130_provenance.