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- source_evidence_literature type ECO_0000212 NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP697182.RA7_5ufeuA-FAemQP_eYpxPHb7e4Fe_CUri-du0XYZsfc130_provenance.