Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_assertion> ?p ?o ?g. }
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- NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_assertion type Assertion NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_head.
- NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_assertion description "[If no causative ENG or ACVRL1 mutation is found, proband samples are referred for sequence analysis of MADH4 (associated with a combined syndrome of juvenile polyposis and HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_provenance.
- NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_assertion evidence source_evidence_literature NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_provenance.
- NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_assertion SIO_000772 16690726 NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_provenance.
- NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_assertion wasDerivedFrom befree-20150227 NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_provenance.
- NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_assertion wasGeneratedBy ECO_0000203 NP222420.RAzkR-R9tm_EX8tG4qMDfGhZtD7CXEW_SHgfnVbDcBw7w130_provenance.