Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP633997.RAR8UD6yE-WFBKvTWpp-NG9HcE60ErhZQ_06PttNiHtP8130_provenance.