Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_assertion> ?p ?o ?g. }
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- NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_assertion type Assertion NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_head.
- NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_assertion description "[HOX genes play a fundamental role in the development of the vertebrate central nervous system, axial skeleton, limbs, gut, urogenital tract and external genitalia, but it is only in the last 4 years that mutations in two of the 39 human HOX genes have been shown to cause congenital malformations; HOXD13, which is mutated in synpolydactyly, and HOXA13, which is mutated in Hand-Foot-Genital syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_provenance.
- NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_assertion evidence source_evidence_literature NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_provenance.
- NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_assertion SIO_000772 11206481 NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_provenance.
- NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_assertion wasDerivedFrom befree-20140225 NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_provenance.
- NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_assertion wasGeneratedBy ECO_0000203 NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_provenance.