Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_assertion> ?p ?o ?g. }
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- NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_assertion type Assertion NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_head.
- NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_assertion description "[NKX2.5 mutations occur in a small percentage of patients with various congenital heart diseases/. 5 mutations in non-homeodomain regions may be important in the development of human structural cardiac defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_provenance.
- NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_assertion evidence source_evidence_literature NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_provenance.
- NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_assertion SIO_000772 14607454 NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_provenance.
- NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_assertion wasDerivedFrom lhgdn-20090331 NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_provenance.
- NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_assertion wasGeneratedBy ECO_0000203 NP185354.RA0cWJduF-IDvSjuWXEXRBd2n04wvmriyPQY66bpeiR5Y130_provenance.