Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_assertion> ?p ?o ?g. }
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- NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_assertion type Assertion NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_head.
- NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_assertion wasGeneratedBy ECO_0000203 NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_provenance.
- NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_assertion wasDerivedFrom befree-20150227 NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_provenance.
- NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_assertion SIO_000772 10698592 NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_provenance.
- NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_assertion evidence source_evidence_literature NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_provenance.
- NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_assertion description "[Inherited adrenocorticotropin (ACTH) insensitivity syndromes comprise a group of rare diseases in which resistance to ACTH is either the sole feature or associated with other symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634427.RAgMyL3RaNP1eXNAA1zZqUfVPm5KaNkAta3IcPTHwVNoI130_provenance.