Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance.
- NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_assertion description "[A novel NTRK1 mutation associated with congenital insensitivity to pain with anhidrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance.
- NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_assertion evidence source_evidence_curated NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance.
- NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_assertion SIO_000772 10090906 NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance.
- NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_assertion wasDerivedFrom uniprot-2016 NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance.
- NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_assertion wasGeneratedBy ECO_0000218 NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP66.RAcEomiugZ-u1aDTdG0h-YHhM-DFCzqzARgpA1I3hfeh4130_provenance.