Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_assertion> ?p ?o ?g. }
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- NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_assertion type Assertion NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_head.
- NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_assertion wasGeneratedBy ECO_0000203 NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_provenance.
- NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_assertion wasDerivedFrom lhgdn-20090331 NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_provenance.
- NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_assertion SIO_000772 14981720 NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_provenance.
- NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_assertion evidence source_evidence_literature NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_provenance.
- NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_assertion description "[A daughter who carried the der Y had the clinical features of Prader-Willi syndrome while a son who carries the der 15 has mild developmental delay and hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203700.RAlbwKlMTYmGwuOtZCAb5p8RIaA39sfE6urXIwKbKd2pQ130_provenance.