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- NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_assertion type Assertion NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_head.
- NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_assertion description "[Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_provenance.
- NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_assertion evidence source_evidence_literature NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_provenance.
- NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_assertion SIO_000772 25646853 NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_provenance.
- NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_assertion wasDerivedFrom befree-2016 NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_provenance.
- NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_assertion wasGeneratedBy ECO_0000203 NP1260590.RAp37m-yfLbeZAYgajK1Tjlitvg3UovYuDgPWfAJCNwf8130_provenance.