Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance.
- NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_assertion wasGeneratedBy ECO_0000203 NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance.
- NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_assertion wasDerivedFrom befree-20150227 NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance.
- NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_assertion SIO_000772 23438977 NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance.
- NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_assertion evidence source_evidence_literature NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance.
- NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_assertion description "[Transthyretin Ala36Pro mutation in a Chinese pedigree of familial transthyretin amyloidosis with elevated vitreous and serum vascular endothelial growth factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761800.RA-7LLLjN3vEVAqpsLKo9CU-a1LaqjF1J4dgHIzYcBqE8130_provenance.