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- source_evidence_literature type ECO_0000212 NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_provenance.
- befree-2016 importedOn "2016-02-19" NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_provenance.
- NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_assertion wasGeneratedBy ECO_0000203 NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_provenance.
- NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_assertion wasDerivedFrom befree-2016 NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_provenance.
- NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_assertion SIO_000772 10835633 NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_provenance.
- NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_assertion evidence source_evidence_literature NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_provenance.
- NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_assertion description "[We have isolated LHX3, a gene involved in a new syndrome, using a candidate-gene approach developed on the basis of documented pituitary abnormalities of a recessive lethal mutation in mice generated by targeted disruption of Lhx3 (ref.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285431.RA2S9Lh1-ctZ75jdgz25vOwRoyNpuqtIP9uwv0RNbK3KM130_provenance.