Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance.
- NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_assertion description "[Genes with potential disease-causing mutations included GNAS, NF2, and RB1, and recurrently mutated genes with unknown roles in tumorigenesis comprised CDC27, SCN7A, and SDK1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance.
- NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_assertion evidence source_evidence_literature NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance.
- NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_assertion SIO_000772 25490274 NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance.
- NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_assertion wasDerivedFrom befree-2016 NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance.
- NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_assertion wasGeneratedBy ECO_0000203 NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246428.RA67kBu7Szhf32k2SUY1J4cizZPkMFvtBhxUWHAeLkPGY130_provenance.