Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_assertion> ?p ?o ?g. }
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- NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_assertion type Assertion NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_head.
- NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_assertion description "[In most case, STS deficiency is caused by a complete or partial deletion of the STS gene mapped on chromosome Xp22.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_provenance.
- NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_assertion evidence source_evidence_curated NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_provenance.
- NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_assertion SIO_000772 14641695 NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_provenance.
- NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_assertion wasDerivedFrom ctd_human-20150221 NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_provenance.
- NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_assertion wasGeneratedBy ECO_0000218 NP31443.RAWOa1ZVGqm0tcJ4Z6q-_fu7zC19DE-uEqL6HlUYrBdSE130_provenance.