Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_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." NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion evidence source_evidence_literature NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion SIO_000772 16912710 NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion wasDerivedFrom befree-20150227 NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion wasGeneratedBy ECO_0000203 NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.