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- source_evidence_literature type ECO_0000212 NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion evidence source_evidence_literature NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion SIO_000772 10982389 NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion wasDerivedFrom befree-20150227 NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion wasGeneratedBy ECO_0000203 NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.