Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.
- NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_assertion description "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.
- NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_assertion evidence source_evidence_literature NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.
- NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_assertion SIO_000772 23731542 NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.
- NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_assertion wasDerivedFrom befree-2016 NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.
- NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_assertion wasGeneratedBy ECO_0000203 NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.