Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_assertion> ?p ?o ?g. }
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- NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_assertion type Assertion NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_head.
- NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_assertion description "[Mutations of the protocadherin19 gene (PCDH19) cause a female-related epilepsy of variable severity, with or without mental retardation and autistic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_provenance.
- NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_assertion evidence source_evidence_literature NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_provenance.
- NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_assertion SIO_000772 22946748 NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_provenance.
- NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_assertion wasDerivedFrom befree-2016 NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_provenance.
- NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_assertion wasGeneratedBy ECO_0000203 NP1010138.RASXr8oOO4ShLR9zx5vT9HeVFUgMlO2ETvzVudE-PLR-w130_provenance.