Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion wasGeneratedBy ECO_0000203 NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion wasDerivedFrom befree-20150227 NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion SIO_000772 12694189 NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion evidence source_evidence_literature NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion description "[Lack of fully functional galactokinase is one cause of the inherited disease galactosemia, the main clinical manifestation of which is early onset cataracts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.