Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance.
- NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_assertion description "[Other malformations associated with MKS3 include cystic changes in the liver, polydactyly, and brain abnormalities (occipital encephalocele, hydrocephalus, and Dandy Walker-type cerebellar anomalies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance.
- NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_assertion evidence source_evidence_literature NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance.
- NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_assertion SIO_000772 19211713 NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance.
- NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_assertion wasDerivedFrom befree-20150227 NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance.
- NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_assertion wasGeneratedBy ECO_0000203 NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP960708.RAqNPNC4GE5nwgFh2zJSZkx8PYpEBTE4rAt41yuYjh3lM130_provenance.