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- source_evidence_literature type ECO_0000212 NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_provenance.
- NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_assertion description "[Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_provenance.
- NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_assertion evidence source_evidence_literature NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_provenance.
- NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_assertion SIO_000772 12704386 NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_provenance.
- NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_assertion wasDerivedFrom befree-2016 NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_provenance.
- NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_assertion wasGeneratedBy ECO_0000203 NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_provenance.
- befree-2016 importedOn "2016-02-19" NP391534.RApE9UDJ6CHr-nqXRPgQogEW3f2j-KiPIbhwna4S5V97s130_provenance.