Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance.
- NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_assertion wasGeneratedBy ECO_0000203 NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance.
- NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_assertion wasDerivedFrom befree-20150227 NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance.
- NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_assertion SIO_000772 23438977 NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance.
- NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_assertion evidence source_evidence_literature NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance.
- NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_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." NP761991.RAXTuoUkbyjq0h82t5YfsdyqrKjEmL2cpwMf9Wxp9NGMY130_provenance.