Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance.
- NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_assertion description "[Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance.
- NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_assertion evidence source_evidence_literature NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance.
- NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_assertion SIO_000772 2571560 NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance.
- NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_assertion wasDerivedFrom befree-20150227 NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance.
- NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_assertion wasGeneratedBy ECO_0000203 NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP737863.RAHxRF7o57qj_QTNL0dFH9qTiMJoWqPL4h4Vc-2DW9cRI130_provenance.