Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.
- NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_assertion description "[Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.
- NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_assertion evidence source_evidence_literature NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.
- NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_assertion SIO_000772 12114496 NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.
- NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_assertion wasDerivedFrom lhgdn-20090331 NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.
- NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_assertion wasGeneratedBy ECO_0000203 NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.