Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_assertion> ?p ?o ?g. }
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- NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_assertion type Assertion NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_head.
- NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_assertion wasGeneratedBy ECO_0000203 NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_provenance.
- NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_assertion wasDerivedFrom befree-20140225 NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_provenance.
- NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_assertion SIO_000772 9748047 NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_provenance.
- NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_assertion evidence source_evidence_literature NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_provenance.
- NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_assertion description "[A Chinese male infant with arthrogryposis multiplex congenita (AMC), ventricular and atrial septal defects, and Werdnig-Hoffmann disease (WHD) had deletions of the telomeric copy of the survival motor neuron (SMN(T)) and neuronal apoptosis inhibitory protein genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP421161.RAC1Tbp5yqDKqqwtcbM0iR89TV6E-jAS6mejkpFqMreMo130_provenance.