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- source_evidence_literature type ECO_0000212 NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_provenance.
- NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_assertion description "[Identification of a novel mutation in the ANGPTL3 gene in two families diagnosed of familial hypobetalipoproteinemia without APOB mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_provenance.
- NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_assertion evidence source_evidence_literature NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_provenance.
- NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_assertion SIO_000772 22155345 NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_provenance.
- NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_assertion wasDerivedFrom befree-20150227 NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_provenance.
- NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_assertion wasGeneratedBy ECO_0000203 NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP889500.RANeZ69F0bmYq4-2LqnfCWxohUT6an5Zgsrz7qOm-bw4w130_provenance.