Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_assertion> ?p ?o ?g. }
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- NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_assertion type Assertion NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_head.
- NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_assertion wasGeneratedBy ECO_0000218 NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_provenance.
- NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_assertion wasDerivedFrom uniprot-20130724 NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_provenance.
- NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_assertion SIO_000772 9694901 NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_provenance.
- NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_assertion evidence source_evidence_curated NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_provenance.
- NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_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." NP3002.RAYRm2OGZqT7LkZK-I7s1Vs19q4gGR8TLzwuVYvVo8YII130_provenance.