Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_assertion> ?p ?o ?g. }
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- NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_assertion type Assertion NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_head.
- NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_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." NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance.
- NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_assertion evidence source_evidence_literature NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance.
- NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_assertion SIO_000772 23029363 NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance.
- NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_assertion wasDerivedFrom befree-20150227 NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance.
- NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_assertion wasGeneratedBy ECO_0000203 NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance.