Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance.
- NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_assertion description "[These findings demonstrate that the spectrum of LAMB2-associated disorders is broader than previously anticipated and includes congenital nephrotic syndrome without eye anomalies or with minor ocular changes different from those observed in Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance.
- NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_assertion evidence source_evidence_literature NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance.
- NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_assertion SIO_000772 16912710 NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance.
- NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_assertion wasDerivedFrom befree-20140225 NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance.
- NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_assertion wasGeneratedBy ECO_0000203 NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717794.RADEol0Fk4lb39vav859gAv2yEBfeWp8c1BT9pvknPSsE130_provenance.