Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion> ?p ?o ?g. }
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- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion type Assertion NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_head.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion wasGeneratedBy ECO_0000203 NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion wasDerivedFrom befree-2016 NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion SIO_000772 23434763 NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion evidence source_evidence_literature NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.
- NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_assertion description "[Recessive inactivating mutations in WNT1 are a new cause of OI type IV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1055311.RA0HMRzYcam1Ci-pEIg65wHL2dq1Ztnjx5TbpuxeUFENk130_provenance.