Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance.
- befree-2016 importedOn "2016-02-19" NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance.
- NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_assertion wasGeneratedBy ECO_0000203 NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance.
- NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_assertion wasDerivedFrom befree-2016 NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance.
- NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_assertion SIO_000772 17943323 NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance.
- NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_assertion evidence source_evidence_literature NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance.
- NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_assertion description "[This observation, together with two recent reports on milder variants of Pierson syndrome, corroborates the concept that the clinical expression of Pierson syndrome is more variable than initially described, and that milder phenotypes may be related to hypomorphic LAMB2 alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635958.RAY18q7c_gB9NSeEfcxyFcWRDCgLNBkTZRVudgla8Ym2E130_provenance.