Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.
- NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_assertion description "[Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive condition unlinked to mutations in SMN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.
- NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_assertion evidence source_evidence_literature NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.
- NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_assertion SIO_000772 22703880 NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.
- NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_assertion wasDerivedFrom befree-20140225 NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.
- NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_assertion wasGeneratedBy ECO_0000203 NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.