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- NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_assertion type Assertion NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_head.
- NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_assertion description "[(4) The test is not recommended for children with phenotypes that are not clearly associated with SCN1A mutations such as those characterized by abnormal development or neurologic deficits apparent at birth or structural abnormalities of the brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_provenance.
- NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_assertion evidence source_evidence_literature NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_provenance.
- NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_assertion SIO_000772 23586701 NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_provenance.
- NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_assertion wasDerivedFrom befree-2016 NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_provenance.
- NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_assertion wasGeneratedBy ECO_0000203 NP1069336.RANseBv1jNexjB0M5tZy4lPYA-NGiIDwKeYuse4UR7-U0130_provenance.