Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.
- NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_assertion wasGeneratedBy ECO_0000203 NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.
- NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_assertion wasDerivedFrom befree-20150227 NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.
- NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_assertion SIO_000772 17177198 NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.
- NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_assertion evidence source_evidence_literature NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.
- NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.