Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_assertion> ?p ?o ?g. }
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- NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_assertion type Assertion NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_head.
- NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_assertion wasGeneratedBy ECO_0000218 NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_provenance.
- NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_assertion wasDerivedFrom uniprot-20150221 NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_provenance.
- NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_assertion SIO_000772 9590296 NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_provenance.
- NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_assertion evidence source_evidence_curated NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_provenance.
- NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_assertion description "[PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3321.RAOLQFRju-_moYX-WH5EGx0kVVp-eqDT9PADmocABwVXc130_provenance.