Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance.
- NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_assertion description "[Recently, mutations in RAF1 have been also identified in patients with NS and two patients with LEOPARD (multiple lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonary stenosis, abnormal genitalia, retardation of growth, and sensorineural deafness) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance.
- NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_assertion evidence source_evidence_literature NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance.
- NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_assertion SIO_000772 20052757 NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance.
- NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_assertion wasDerivedFrom befree-20150227 NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance.
- NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_assertion wasGeneratedBy ECO_0000203 NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP664333.RAHH8I80zCV5lgocl0EvSyC_XTvVLbsGAzYltJ1t5Jc4E130_provenance.