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- source_evidence_literature type ECO_0000212 NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.
- NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.
- NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_assertion evidence source_evidence_literature NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.
- NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_assertion SIO_000772 20949531 NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.
- NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_assertion wasDerivedFrom befree-20150227 NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.
- NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_assertion wasGeneratedBy ECO_0000203 NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.
- befree-20150227 importedOn "2015-02-27" NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.