Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance.
- NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_assertion description "[Patients with confirmed FLN-1 gene mutations are usually female and have a distinctive MR pattern of PNH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance.
- NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_assertion evidence source_evidence_literature NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance.
- NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_assertion SIO_000772 11100490 NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance.
- NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_assertion wasDerivedFrom befree-20150227 NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance.
- NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_assertion wasGeneratedBy ECO_0000203 NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP406858.RAD0y9IYYETeQhHCj6cqRn2vT4_9TrhYQoUIa4e8IJG8w130_provenance.