Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_assertion> ?p ?o ?g. }
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- NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_assertion type Assertion NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_head.
- NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_assertion description "[A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_provenance.
- NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_assertion evidence source_evidence_literature NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_provenance.
- NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_assertion SIO_000772 17646629 NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_provenance.
- NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_assertion wasDerivedFrom befree-2016 NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_provenance.
- NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_assertion wasGeneratedBy ECO_0000203 NP621334.RAMzPNZHRRFARqnTcoNpxhP5pjcwsK4kvyK5b50cRM3Vs130_provenance.