Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance.
- NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_assertion description "[HPTH has been associated with a number of familial diseases, such as multiple endocrine neoplasia-type 1 (MEN1), multiple endocrine neoplasia-type2A (MEN2A), neurofibromatosis type1 (NF1) and HPTH with multiple ossifying jaw fibromas (HPT-JT Syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance.
- NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_assertion evidence source_evidence_literature NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance.
- NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_assertion SIO_000772 16299679 NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance.
- NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_assertion wasDerivedFrom befree-2016 NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance.
- NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_assertion wasGeneratedBy ECO_0000203 NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance.
- befree-2016 importedOn "2016-02-19" NP523354.RA6C0HZN02_e4ED1CIGNZ0gLhQTuNDAz3fr4sJnwuXGTo130_provenance.