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- source_evidence_literature type ECO_0000212 NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_provenance.
- NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_assertion description "[Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes (USH2A, USH2B, and USH2C) and is classified phenotypically as congenital hearing loss and progressive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_provenance.
- NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_assertion evidence source_evidence_literature NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_provenance.
- NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_assertion SIO_000772 14740321 NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_provenance.
- NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_assertion wasDerivedFrom befree-20150227 NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_provenance.
- NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_assertion wasGeneratedBy ECO_0000203 NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP954504.RAwPPOyzBVwxu7nmoAnEqTY1fD4RCzKdvRQl_FzmDp7pc130_provenance.