Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_assertion> ?p ?o ?g. }
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- NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_assertion type Assertion NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_head.
- NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_assertion description "[GCMB is a parathyroid-specific transcription factor, which causes hypoparathyroidism when inactivated on both parental alleles or when a dominant-negative, heterozygous mutation is present.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_provenance.
- NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_assertion evidence source_evidence_literature NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_provenance.
- NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_assertion SIO_000772 21642377 NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_provenance.
- NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_assertion wasDerivedFrom befree-2016 NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_provenance.
- NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_assertion wasGeneratedBy ECO_0000203 NP899501.RAJoqcj9NMEky2qUHzQNqFfr3Ic1ex6IHKhjKNwgAYPs4130_provenance.