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- source_evidence_literature type ECO_0000212 NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_provenance.
- NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_assertion description "[Recessive MLC1 mutations are observed in 75% of patients with MLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_provenance.
- NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_assertion evidence source_evidence_literature NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_provenance.
- NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_assertion SIO_000772 21419380 NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_provenance.
- NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_assertion wasDerivedFrom befree-20150227 NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_provenance.
- NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_assertion wasGeneratedBy ECO_0000203 NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583891.RAY-pvd7f0wEe88-pZJS38YTHtpI8aerjVzFSxBJ9sKnA130_provenance.