Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP455195.RAbmZWuTWjnaZCFmn2yjMA64fUsPpNKNzp1VH8oON1QdI130_provenance.