Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance.
- NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_assertion description "[A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance.
- NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_assertion evidence source_evidence_literature NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance.
- NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_assertion SIO_000772 23611888 NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance.
- NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_assertion wasDerivedFrom befree-2016 NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance.
- NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_assertion wasGeneratedBy ECO_0000203 NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1071677.RA_qrH7fWbnbH7oSjKuJ93MCBpZpWuQbz83k2m54Re75Y130_provenance.