Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance.
- NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_assertion description "[Here, we review the clinical characteristics of the MEN4 syndrome and the molecular phenotype of the associated p27Kip1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance.
- NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_assertion evidence source_evidence_literature NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance.
- NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_assertion SIO_000772 23652671 NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance.
- NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_assertion wasDerivedFrom befree-20140225 NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance.
- NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_assertion wasGeneratedBy ECO_0000203 NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718547.RAoLu5WOq61QBvSK61D2wDuj4eSz-iyGZy5FvigHL-8U8130_provenance.