Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion> ?p ?o ?g. }
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- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion type Assertion NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_head.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion wasGeneratedBy ECO_0000203 NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion wasDerivedFrom befree-2016 NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion SIO_000772 9694901 NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion evidence source_evidence_literature NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion description "[We have previously reported two sisters with chronic Sandhoff disease who were heterozygous for the common HEXB deletion allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.