Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_assertion> ?p ?o ?g. }
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- NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_assertion type Assertion NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_head.
- NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_assertion wasGeneratedBy ECO_0000203 NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance.
- NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_assertion wasDerivedFrom befree-20150227 NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance.
- NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_assertion SIO_000772 12798584 NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance.
- NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_assertion evidence source_evidence_literature NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance.
- NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_assertion description "[Screening for NKX2-5 mutations may be warranted in individuals with ASD and a positive family history, irrespective of the presence or absence of AV conduction block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance.