Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance.
- NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_assertion description "[reported a separate family with X-linked recessive spastic paraplegia and mental retardation and demonstrated close linkage to DXS15 and DXS52 (DX13 and St14) at Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance.
- NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_assertion evidence source_evidence_literature NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance.
- NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_assertion SIO_000772 2737668 NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance.
- NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_assertion wasDerivedFrom befree-20150227 NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance.
- NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_assertion wasGeneratedBy ECO_0000203 NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP715198.RAfUdyi8LsHf_W-z_ihbLcWl13Nhw_RJKTS_FJmfpQbXc130_provenance.