Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion> ?p ?o ?g. }
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- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion type Assertion NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_head.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion description "[Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion evidence source_evidence_literature NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion SIO_000772 15389319 NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion wasDerivedFrom befree-20150227 NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion wasGeneratedBy ECO_0000203 NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.