Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance.
- NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_assertion description "[A mutation analysis of GRB10 in 58 unrelated patients with RSS identified, within the N-terminal domain of the protein, a P95S substitution in two patients with RSS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance.
- NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_assertion evidence source_evidence_literature NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance.
- NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_assertion SIO_000772 10856193 NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance.
- NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_assertion wasDerivedFrom befree-20140225 NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance.
- NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_assertion wasGeneratedBy ECO_0000203 NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP646593.RAfMIkkrpdocsEVvsEdux8-2lYZ5xTTi_d8yY6fipyEpY130_provenance.