Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance.
- NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_assertion description "[Further investigation revealed low levels of the glycoproteins AT III and clotting factor XI, leading to a diagnosis of congenital disorder of glycosylation (CDG) type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance.
- NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_assertion evidence source_evidence_literature NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance.
- NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_assertion SIO_000772 19067230 NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance.
- NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_assertion wasDerivedFrom befree-20150227 NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance.
- NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_assertion wasGeneratedBy ECO_0000203 NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP254291.RA22Pat5Md4Twl7LF030BcQ9Bfmqw2N9artO73d8Q19QM130_provenance.