Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion> ?p ?o ?g. }
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- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion type Assertion NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_head.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion description "[A deletion of Asn169 in the peripherin/RDS protein causes a peculiar form of autosomal dominant macular dystrophy in a large family from the Netherlands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion evidence source_evidence_literature NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion SIO_000772 14557182 NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion wasDerivedFrom befree-20150227 NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion wasGeneratedBy ECO_0000203 NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.