Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_assertion> ?p ?o ?g. }
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- NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_assertion type Assertion NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_head.
- NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_assertion description "[Mutations in transcription factor NKX2.5 cause congenital heart disease (CHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_provenance.
- NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_assertion evidence source_evidence_literature NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_provenance.
- NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_assertion SIO_000772 20932824 NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_provenance.
- NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_assertion wasDerivedFrom befree-2016 NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_provenance.
- NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_assertion wasGeneratedBy ECO_0000203 NP844560.RAhRvb8425UJkdSTbUnLju4pdz1TCm2OroTBhkqhB4lAs130_provenance.