Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance.
- NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_assertion wasGeneratedBy ECO_0000203 NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance.
- NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_assertion wasDerivedFrom lhgdn-20090331 NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance.
- NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_assertion SIO_000772 14981720 NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance.
- NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_assertion evidence source_evidence_literature NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance.
- NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_assertion description "[A daughter who carried the der Y had the clinical features of Prader-Willi syndrome while a son who carries the der 15 has mild developmental delay and hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203701.RA7n9ZeSBxQRMZ6row-V0-1o4Pt3bmZnFfhFsBbpZIFSs130_provenance.