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- NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_assertion type Assertion NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_head.
- NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_assertion description "[The basic molecular work-up included analysis of concordance based on 10 polymorphic markers (D3S1358, vVA, FGA, amelogenin, D8S1179, D21S11, D18S51, D5S818, D13S317, D7S820) and exclusion of the major slit-diaphragm gene mutation (NPHS2, CD2AP, WT1) causing nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_provenance.
- NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_assertion evidence source_evidence_literature NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_provenance.
- NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_assertion SIO_000772 16382323 NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_provenance.
- NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_assertion wasDerivedFrom befree-20150227 NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_provenance.
- NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_assertion wasGeneratedBy ECO_0000203 NP876357.RA0Bxvi7Vjck_DsKghhls1hd3ahz6h4AZ1NI4Esjx5LvE130_provenance.