Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance.
- NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_assertion description "[Mutations in the gene encoding profilin 1 (PFN1) have recently been shown to cause amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance.
- NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_assertion evidence source_evidence_literature NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance.
- NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_assertion SIO_000772 25499087 NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance.
- NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_assertion wasDerivedFrom befree-2016 NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance.
- NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_assertion wasGeneratedBy ECO_0000203 NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247139.RA9wNja6fbiX2pn2iShem4hOOiSEo3jgvIf1R7MRKv6RU130_provenance.