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- source_evidence_literature type ECO_0000212 NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_provenance.
- NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_assertion description "[Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_provenance.
- NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_assertion evidence source_evidence_literature NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_provenance.
- NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_assertion SIO_000772 16648375 NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_provenance.
- NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_assertion wasDerivedFrom befree-2016 NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_provenance.
- NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_assertion wasGeneratedBy ECO_0000203 NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_provenance.
- befree-2016 importedOn "2016-02-19" NP547518.RA1uLcd7Dx5mbzKIOpcjAS1huClhdOYpWvekE9kqH94LE130_provenance.