Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.
- NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.
- NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_assertion evidence source_evidence_literature NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.
- NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_assertion SIO_000772 11275328 NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.
- NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_assertion wasDerivedFrom befree-2016 NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.
- NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_assertion wasGeneratedBy ECO_0000203 NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.