Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance.
- NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_assertion description "[Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance.
- NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_assertion evidence source_evidence_curated NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance.
- NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_assertion SIO_000772 22158539 NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance.
- NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_assertion wasDerivedFrom uniprot-20130724 NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance.
- NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_assertion wasGeneratedBy ECO_0000218 NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6232.RAgUhEHoGbXfhuL6IK7YQCDnq8Jr57E9LxrlK1HNoI2ro130_provenance.