Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_assertion> ?p ?o ?g. }
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- NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_assertion type Assertion NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_head.
- NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_assertion description "[We performed STRA6 molecular analysis in three fetuses and one child diagnosed with Matthew-Wood syndrome and in three siblings where two adult living brothers are affected with combinations of clinical anophthalmia, tetralogy of Fallot, and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_provenance.
- NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_assertion evidence source_evidence_literature NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_provenance.
- NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_assertion SIO_000772 19309693 NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_provenance.
- NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_assertion wasDerivedFrom befree-2016 NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_provenance.
- NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_assertion wasGeneratedBy ECO_0000203 NP728022.RAd28paHxDrqHs_kE0nZDOkZYhKQ6P5vbkQvcgkSTWKYc130_provenance.