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- source_evidence_literature type ECO_0000212 NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.
- NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_assertion description "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.
- NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_assertion evidence source_evidence_literature NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.
- NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_assertion SIO_000772 16912710 NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.
- NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_assertion wasDerivedFrom befree-20140225 NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.
- NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_assertion wasGeneratedBy ECO_0000203 NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.