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- source_evidence_literature type ECO_0000212 NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.
- NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.
- NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_assertion evidence source_evidence_literature NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.
- NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_assertion SIO_000772 18499664 NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.
- NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_assertion wasDerivedFrom befree-2016 NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.
- NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_assertion wasGeneratedBy ECO_0000203 NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.
- befree-2016 importedOn "2016-02-19" NP672830.RAz_bYstp7o0AkJBf2AX08SJ2MBw9JDXcZlO775MToR7c130_provenance.