Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_assertion> ?p ?o ?g. }
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- NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_assertion type Assertion NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_head.
- NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_assertion description "[Similarly, mutations in the human CFC1 gene have been identified in patients with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_provenance.
- NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_assertion evidence source_evidence_literature NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_provenance.
- NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_assertion SIO_000772 17072672 NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_provenance.
- NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_assertion wasDerivedFrom befree-20140225 NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_provenance.
- NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_assertion wasGeneratedBy ECO_0000203 NP745075.RAhd62dLUEtrobOmCuiieyGTuFmotcCMh0s1BaHThLiDM130_provenance.