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- NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_assertion type Assertion NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_head.
- NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_provenance.
- NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_assertion evidence source_evidence_literature NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_provenance.
- NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_assertion SIO_000772 2564060 NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_provenance.
- NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_assertion wasDerivedFrom befree-2016 NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_provenance.
- NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_assertion wasGeneratedBy ECO_0000203 NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_provenance.