Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance.
- NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_assertion description "[Mutations in the GDAP1 gene are responsible of the Charcot-Marie-Tooth CMT4A, ARCMT2K, and CMT2K variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance.
- NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_assertion evidence source_evidence_literature NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance.
- NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_assertion SIO_000772 21890626 NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance.
- NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_assertion wasDerivedFrom befree-2016 NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance.
- NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_assertion wasGeneratedBy ECO_0000203 NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance.
- befree-2016 importedOn "2016-02-19" NP921350.RAv9WRMbnt2Jee2Jns-qG2U0In7CRLTQD4hOKQw8nlNO4130_provenance.