Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance.
- NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_assertion description "[Differential diagnosis involves the exclusion of mild hypothyroidism in autoimmune thyroid disease or pseudohypoparathyroidism associated with genetic or epigenetic defects at the GNAS locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance.
- NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_assertion evidence source_evidence_literature NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance.
- NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_assertion SIO_000772 20083154 NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance.
- NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_assertion wasDerivedFrom befree-20140225 NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance.
- NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_assertion wasGeneratedBy ECO_0000203 NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP504655.RAOt_7qmf3d5Jn24uO5QybMZ8JLJgW6ocsQt33GqEX_2g130_provenance.