Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance.
- NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_assertion description "[Mapping of transforming growth factor alpha gene on human chromosome 2 close to the breakpoint of the Burkitt's lymphoma t(2;8) variant translocation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance.
- NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_assertion evidence source_evidence_literature NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance.
- NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_assertion SIO_000772 3863708 NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance.
- NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_assertion wasDerivedFrom befree-20140225 NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance.
- NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_assertion wasGeneratedBy ECO_0000203 NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477789.RAXt6HA3qMv7vRtoLZOjPMF-eOSQX71YI1xlgKnerWwfg130_provenance.