Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance.
- NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_assertion description "[Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance.
- NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_assertion evidence source_evidence_literature NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance.
- NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_assertion SIO_000772 23029363 NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance.
- NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_assertion wasDerivedFrom befree-20140225 NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance.
- NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_assertion wasGeneratedBy ECO_0000203 NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP913973.RA7m9BVZU6-M45z43L87ZuHTAVVgoSoPnnw8taEWKkdq0130_provenance.