Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP334003.RAonN2Gc3R6onDFBAkcY-7_njZ91BAlPhK4TVgUWc8M-k130_provenance.
- 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.