Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_assertion type Assertion NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_head.
- NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_assertion description "[Hereditary spastic paraparesis (HPS) linked to mutations in the spastin gene (SPG4) is considered to be a pure form of spastic hereditary paraparesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance.
- NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_assertion evidence source_evidence_literature NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance.
- NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_assertion SIO_000772 19289482 NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance.
- NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_assertion wasDerivedFrom befree-20140225 NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance.
- NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_assertion wasGeneratedBy ECO_0000203 NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance.