Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance.
- NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_assertion description "[In transthyretin (TTR) a new mutation (TTR-Thr45) has been identified in a patient with familial amyloidosis characterized clinically by prominent cardiomyopathy and the absence of peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance.
- NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_assertion evidence source_evidence_literature NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance.
- NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_assertion SIO_000772 1570831 NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance.
- NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_assertion wasDerivedFrom befree-2016 NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance.
- NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_assertion wasGeneratedBy ECO_0000203 NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance.
- befree-2016 importedOn "2016-02-19" NP480687.RANca1PT311MN5BQPjZR1pwUx5aGsKPHSHjW6PvGHN1zk130_provenance.