Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_assertion type Assertion NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_head.
- NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_provenance.
- NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_assertion evidence source_evidence_literature NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_provenance.
- NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_assertion SIO_000772 19854292 NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_provenance.
- NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_assertion wasDerivedFrom befree-2016 NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_provenance.
- NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_assertion wasGeneratedBy ECO_0000203 NP771461.RA7KtnKMvJJSupuTrYxVOqGAhzoU2WJwBlLquFaIOr_tE130_provenance.