Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_assertion> ?p ?o ?g. }
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- NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_assertion type Assertion NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_head.
- NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_assertion wasGeneratedBy ECO_0000203 NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_provenance.
- NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_assertion wasDerivedFrom befree-20150227 NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_provenance.
- NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_assertion SIO_000772 15965158 NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_provenance.
- NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_assertion evidence source_evidence_literature NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_provenance.
- NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_assertion description "[The data indicate that the novel mutation 640C>T in the OA1 gene is the primary cause of the eye disease in the family studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002272.RATTHNUBpOsyWGc2zkTR4cmsDAuclp0nEsMRgW8T4G2h4130_provenance.