Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance.
- NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_assertion description "[Interestingly, in the largest SAX2 family, the presenting clinical sign was dysarthria, which is not common in other forms of inherited ataxias or spastic ataxias, whereas gait difficulties appeared later.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance.
- NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_assertion evidence source_evidence_literature NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance.
- NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_assertion SIO_000772 17273843 NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance.
- NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_assertion wasDerivedFrom befree-20150227 NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance.
- NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_assertion wasGeneratedBy ECO_0000203 NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP913386.RAen6kwP_A9y8WtvRIsxC7jWfEUS0tRKh9Y9VPpdEHcvg130_provenance.