Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.
- befree-2016 importedOn "2016-02-19" NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.
- NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_assertion wasGeneratedBy ECO_0000203 NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.
- NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_assertion wasDerivedFrom befree-2016 NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.
- NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_assertion SIO_000772 18989701 NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.
- NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_assertion evidence source_evidence_literature NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.
- NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.