Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance.
- NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_assertion description "[NKX2.5 mutations in patients with congenital heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance.
- NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_assertion evidence source_evidence_literature NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance.
- NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_assertion SIO_000772 14607454 NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance.
- NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_assertion wasDerivedFrom befree-2016 NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance.
- NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_assertion wasGeneratedBy ECO_0000203 NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance.
- befree-2016 importedOn "2016-02-19" NP419890.RAeUjn6OLSDO5NWmzMYsU28Do1YG5SL1P00w8WR8XAf4o130_provenance.