Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance.
- NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_assertion description "[The current study expands the spectrum of allelic variants in SPG4, confirming their pathological significance in pure AD-HSP and suggesting implications for the presumed function of spastin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance.
- NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_assertion evidence source_evidence_curated NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance.
- NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_assertion SIO_000772 11985387 NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance.
- NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_assertion wasDerivedFrom uniprot-2016 NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance.
- NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_assertion wasGeneratedBy ECO_0000218 NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP2002.RAG2YTvnmrhY0KLWF14HXBczf8H50JC7ZBjOev9CyzfU8130_provenance.