Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance.
- NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_assertion description "[PTEN hamartoma tumour syndrome (PHTS) encompasses several clinical syndromes with germline mutations in the PTEN tumour suppressor gene, including Cowden syndrome which is characterised by an increased risk of breast and thyroid cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance.
- NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_assertion evidence source_evidence_literature NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance.
- NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_assertion SIO_000772 23335809 NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance.
- NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_assertion wasDerivedFrom befree-2016 NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance.
- NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_assertion wasGeneratedBy ECO_0000203 NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1045500.RARlhACXW8ff6F6_jIaLt8a2wGW4yl2gWLWCcnhiyP6rM130_provenance.