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- source_evidence_literature type ECO_0000212 NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.
- NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_assertion description "[Mutations in MECP2, encoding methyl CpG binding protein 2 (MeCP2), cause most cases of Rett syndrome (RTT), an X-linked neurodevelopmental disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.
- NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_assertion evidence source_evidence_literature NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.
- NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_assertion SIO_000772 17486179 NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.
- NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_assertion wasDerivedFrom befree-2016 NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.
- NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_assertion wasGeneratedBy ECO_0000203 NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.
- befree-2016 importedOn "2016-02-19" NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.