Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.
- NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_assertion description "[The infant was found to be heterozygous for the prothrombin G20210A mutation and homozygous for the methylenetetrahydrofolate reductase C667T mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.
- NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_assertion evidence source_evidence_literature NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.
- NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_assertion SIO_000772 13679943 NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.
- NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_assertion wasDerivedFrom befree-2016 NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.
- NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_assertion wasGeneratedBy ECO_0000203 NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.
- befree-2016 importedOn "2016-02-19" NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.