Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance.
- NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_assertion description "[Besides, there is no report about the association between NBS1 3'UTR variant rs2735383 and ALL risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance.
- NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_assertion evidence source_evidence_literature NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance.
- NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_assertion SIO_000772 21166880 NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance.
- NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_assertion wasDerivedFrom befree-20150227 NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance.
- NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_assertion wasGeneratedBy ECO_0000203 NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP432001.RAm5nLe4EW0tespHoqEx0Sx0TX1CHsRFgQ4CrQj8I70rg130_provenance.