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- source_evidence_literature type ECO_0000212 NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_provenance.
- NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_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." NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_provenance.
- NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_assertion evidence source_evidence_literature NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_provenance.
- NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_assertion SIO_000772 23029363 NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_provenance.
- NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_assertion wasDerivedFrom befree-20140225 NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_provenance.
- NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_assertion wasGeneratedBy ECO_0000203 NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP207996.RAsJkS-pJhhDGyzlAo2KmE_DSigYF_mZL9xwfN0JLoXD8130_provenance.