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- source_evidence_literature type ECO_0000212 NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.
- NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_assertion description "[Rett syndrome (RTT) is caused by mutations of MECP2, a methyl CpG binding protein thought to act as a global transcriptional repressor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.
- NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_assertion evidence source_evidence_literature NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.
- NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_assertion SIO_000772 24094325 NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.
- NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_assertion wasDerivedFrom befree-20150227 NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.
- NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_assertion wasGeneratedBy ECO_0000203 NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.