Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance.
- NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_assertion description "[Mutations in the Notch pathway ligand Jagged1 (JAG1) cause Alagille syndrome (AGS), as well as cardiac defects in seemingly nonsyndromic individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance.
- NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_assertion evidence source_evidence_literature NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance.
- NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_assertion SIO_000772 20437614 NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance.
- NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_assertion wasDerivedFrom befree-2016 NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance.
- NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_assertion wasGeneratedBy ECO_0000203 NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP809766.RAUjBhxDO4i6JGM8WcwUV_nG-kie4I9ASYASUbqZGN12Y130_provenance.