Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance.
- NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_assertion description "[We screened 120 children with sporadic multiple congenital anomalies and either growth or mental retardation for uniparental disomy (UPD) or subtelomeric deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance.
- NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_assertion evidence source_evidence_literature NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance.
- NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_assertion SIO_000772 11702212 NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance.
- NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_assertion wasDerivedFrom befree-20140225 NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance.
- NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_assertion wasGeneratedBy ECO_0000203 NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP775578.RAQvqaw2B7WjSD9cjRcAZ8nebE32ToHpMYYYXyHQeJylw130_provenance.