Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_assertion> ?p ?o ?g. }
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- NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_assertion type Assertion NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_head.
- NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_assertion description "[Null-allele mutations in the COL2A1 gene led to a typical phenotype of Stickler syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_provenance.
- NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_assertion evidence source_evidence_literature NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_provenance.
- NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_assertion SIO_000772 10486316 NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_provenance.
- NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_assertion wasDerivedFrom befree-2016 NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_provenance.
- NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_assertion wasGeneratedBy ECO_0000203 NP263014.RALDu8utKk0vDaKDsSN-qY0B02Jp16AgXzqR4KH_Z1ETs130_provenance.