Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance.
- NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_assertion description "[MECP2 mutations have also been identified in individuals with a variety of clinical syndromes, including mild learning-disability in females, neonatal encephalopathy in males, and psychiatric disorders, autism and X-linked mental retardation in both males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance.
- NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_assertion evidence source_evidence_literature NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance.
- NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_assertion SIO_000772 16647848 NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance.
- NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_assertion wasDerivedFrom befree-2016 NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance.
- NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_assertion wasGeneratedBy ECO_0000203 NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance.
- befree-2016 importedOn "2016-02-19" NP547448.RAcZRz_RZpIJxPDGRxRpbt4vFo-qmvd6ENI1w0qDevpzE130_provenance.