Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_assertion> ?p ?o ?g. }
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- NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_assertion type Assertion NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_head.
- 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.