Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance.
- NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_assertion description "[A novel missense mutation (P366T) of the LHX4 gene causes severe combined pituitary hormone deficiency with pituitary hypoplasia, ectopic posterior lobe and a poorly developed sella turcica.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance.
- NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_assertion evidence source_evidence_literature NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance.
- NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_assertion SIO_000772 17527005 NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance.
- NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_assertion wasDerivedFrom befree-20150227 NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance.
- NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_assertion wasGeneratedBy ECO_0000203 NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP960078.RAQmBYEwsnGibCvRpwkH5l8M3TcUP_wSdXmQ1fv_bJ89c130_provenance.