Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_assertion> ?p ?o ?g. }
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- NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_assertion type Assertion NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_head.
- NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_assertion description "[Mutations in the genes encoding ATP7A and ATP7B lead to copper deficiency and toxicity disorders, Menkes and Wilson diseases, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_provenance.
- NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_assertion evidence source_evidence_literature NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_provenance.
- NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_assertion SIO_000772 21242307 NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_provenance.
- NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_assertion wasDerivedFrom befree-20140225 NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_provenance.
- NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_assertion wasGeneratedBy ECO_0000203 NP713968.RA04m2mRnf8XlWc95XU6Nau04wKYBTzL-wHuLlgt_W0MA130_provenance.