Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance.
- NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_assertion description "[MECP2 mutations in large groups of males and females affected with mental retardation without FRAXA expansion ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance.
- NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_assertion evidence source_evidence_literature NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance.
- NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_assertion SIO_000772 17383248 NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance.
- NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_assertion wasDerivedFrom lhgdn-20090331 NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance.
- NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_assertion wasGeneratedBy ECO_0000203 NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP189995.RA53v_pzFuAugwndEfWczy5JTO4WFGGMv9Qhv62bxpJFM130_provenance.