Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance.
- befree-2016 importedOn "2016-02-19" NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance.
- NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_assertion wasGeneratedBy ECO_0000203 NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance.
- NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_assertion wasDerivedFrom befree-2016 NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance.
- NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_assertion SIO_000772 20949621 NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance.
- NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_assertion evidence source_evidence_literature NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance.
- NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_assertion description "[Germline KRAS mutations were shown recently to be associated with developmental disorders, including Noonan syndrome (NS), cardio-facio-cutaneous syndrome (CFCS), and Costello syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845911.RAdO8KcuH4JvFRHAVWIzOJxikdm1uJLrb1pNcoR2422Uw130_provenance.