Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance.
- NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_assertion description "[Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia. Mutations in brief no. 164. Online.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance.
- NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_assertion evidence source_evidence_curated NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance.
- NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_assertion SIO_000772 10694922 NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance.
- NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_assertion wasDerivedFrom uniprot-2016 NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance.
- NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_assertion wasGeneratedBy ECO_0000218 NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP666.RARWVYCSSLK_DQthjab2rkhE10i0aVj_aL8SRiUfCeeIc130_provenance.