Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance.
- befree-2016 importedOn "2016-02-19" NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance.
- NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_assertion wasGeneratedBy ECO_0000203 NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance.
- NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_assertion wasDerivedFrom befree-2016 NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance.
- NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_assertion SIO_000772 15953452 NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance.
- NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_assertion evidence source_evidence_literature NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance.
- NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_assertion description "[These findings fit the haplotype analysis that we reported previously and indicate that the predicted protein that is encoded by CHST6 is more severely affected in the individual with MCD type I than in the siblings with MCD type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499265.RANV8BZsfUQ0dbdHi_8cfNpNETI6SRlVvX8EWvMtovUlE130_provenance.