Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion> ?p ?o ?g. }
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- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion type Assertion NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_head.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion description "[The patient is heterozygous for an alteration in the A2M gene; this may be responsible for his serum A2M deficiency and may be relevant to the early onset of pulmonary disease in his case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion evidence source_evidence_literature NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion SIO_000772 2475424 NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion wasDerivedFrom befree-2016 NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion wasGeneratedBy ECO_0000203 NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.