Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.
- NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_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." NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.
- NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_assertion evidence source_evidence_literature NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.
- NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_assertion SIO_000772 16912710 NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.
- NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_assertion wasDerivedFrom befree-20150227 NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.
- NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_assertion wasGeneratedBy ECO_0000203 NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.