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- source_evidence_literature type ECO_0000212 NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_provenance.
- NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_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." NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_provenance.
- NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_assertion evidence source_evidence_literature NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_provenance.
- NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_assertion SIO_000772 16647848 NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_provenance.
- NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_assertion wasDerivedFrom befree-20150227 NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_provenance.
- NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_assertion wasGeneratedBy ECO_0000203 NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP552141.RAUy4NQJAaivh9VhC08W9Zy-nhUSoaLdpXwrzxeAsFX4w130_provenance.