Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_assertion> ?p ?o ?g. }
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- NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_assertion type Assertion NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_head.
- NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_assertion wasGeneratedBy ECO_0000218 NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_provenance.
- NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_assertion wasDerivedFrom ctd_human-2016 NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_provenance.
- NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_assertion SIO_000772 15146389 NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_provenance.
- NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_assertion evidence source_evidence_curated NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_provenance.
- NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_assertion description "[A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14122.RAoKe3W1hO2hXmyv6uelz1C6Hf4_UODLAerivqnVmWgvw130_provenance.