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- source_evidence_literature type ECO_0000212 NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_provenance.
- NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_assertion description "[Mutations in the coding sequence of the methyl-CpG-binding protein 2 gene (MECP2), which cause Rett syndrome (RTT), have been found in male and female autistic subjects without, however, a causal relation having unequivocally been established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_provenance.
- NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_assertion evidence source_evidence_literature NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_provenance.
- NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_assertion SIO_000772 17427193 NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_provenance.
- NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_assertion wasDerivedFrom befree-2016 NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_provenance.
- NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_assertion wasGeneratedBy ECO_0000203 NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_provenance.
- befree-2016 importedOn "2016-02-19" NP603980.RAICpGrCMQSG8D4Cwnuw07oRYpdHZoTxUVTpfcKjEZZnw130_provenance.