Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion type Assertion NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_head.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion description "[A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion evidence source_evidence_literature NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion SIO_000772 18445675 NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion wasDerivedFrom befree-20150227 NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.
- NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_assertion wasGeneratedBy ECO_0000203 NP960060.RAWB8a4vprEOfEeo7CPaDDElpnbKRccrt_s_d2He6mZgo130_provenance.