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- NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_assertion type Assertion NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_head.
- NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_assertion description "[A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_provenance.
- NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_assertion evidence source_evidence_literature NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_provenance.
- NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_assertion SIO_000772 23065719 NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_provenance.
- NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_assertion wasDerivedFrom befree-20140225 NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_provenance.
- NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_assertion wasGeneratedBy ECO_0000203 NP676850.RAYLTMXpAsCj1_a91G0Q8-505SvaHX-tMj7zZf5GTfjYw130_provenance.