Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance.
- NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_assertion description "[However, in one family (MRX19), a missense mutation was associated solely with mild mental retardation and no other clinical feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance.
- NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_assertion evidence source_evidence_literature NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance.
- NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_assertion SIO_000772 11896450 NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance.
- NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_assertion wasDerivedFrom befree-2016 NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance.
- NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_assertion wasGeneratedBy ECO_0000203 NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance.
- befree-2016 importedOn "2016-02-19" NP348269.RAL3WJSNFXotVtAESl6KrrPtN4dZOyfyGEtz0J50HyY28130_provenance.