Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance.
- NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_assertion description "[Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance.
- NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_assertion evidence source_evidence_curated NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance.
- NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_assertion SIO_000772 24951643 NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance.
- NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_assertion wasDerivedFrom uniprot-20150221 NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance.
- NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_assertion wasGeneratedBy ECO_0000218 NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP46.RAnwfzN8zAI3ax8le-wHFDXcYp8r-Uv37mXTRjepeTfy8130_provenance.