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- source_evidence_literature type ECO_0000212 NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_provenance.
- NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_assertion description "[Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_provenance.
- NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_assertion evidence source_evidence_literature NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_provenance.
- NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_assertion SIO_000772 12893758 NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_provenance.
- NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_assertion wasDerivedFrom befree-2016 NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_provenance.
- NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_assertion wasGeneratedBy ECO_0000203 NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_provenance.
- befree-2016 importedOn "2016-02-19" NP403993.RAm2BKoN1KL5Jj5nb91v_A2Zk02RHkztVa4-5fQRgAmoc130_provenance.