Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance.
- NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_assertion description "[DNA analysis showed heterozygosity for normal TTR and the amyloidogenic mutation ATTR (Val30Met) leading to the diagnosis of familial amyloidotic polyneuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance.
- NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_assertion evidence source_evidence_literature NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance.
- NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_assertion SIO_000772 12082059 NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance.
- NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_assertion wasDerivedFrom lhgdn-20090331 NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance.
- NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_assertion wasGeneratedBy ECO_0000203 NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP194983.RATzgFA2I2LEzGevd4G2PUa1NY-ul6MaSX642-1T6NxcA130_provenance.