Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion description "[Rett syndrome (RTT) is a neurodevelopmental disorder mostly caused by MECP2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion evidence source_evidence_literature NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion SIO_000772 24621584 NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion wasDerivedFrom befree-2016 NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion wasGeneratedBy ECO_0000203 NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.