Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion> ?p ?o ?g. }
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- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion type Assertion NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_head.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion evidence source_evidence_literature NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion SIO_000772 23872636 NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion wasDerivedFrom befree-20150227 NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion wasGeneratedBy ECO_0000203 NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.