Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance.
- NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_assertion description "[In more than 80% of XLI patients the enzyme deficiency is due to large deletions involving the entire STS gene and flanking sequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance.
- NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_assertion evidence source_evidence_literature NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance.
- NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_assertion SIO_000772 1539590 NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance.
- NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_assertion wasDerivedFrom befree-20150227 NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance.
- NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_assertion wasGeneratedBy ECO_0000203 NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP253095.RALmh5HcsjPshlAsL-aWaUoTiKX4wd4zX-pCR87-qhlwM130_provenance.