Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion description "[Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion evidence source_evidence_literature NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion SIO_000772 21340158 NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion wasDerivedFrom befree-2016 NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion wasGeneratedBy ECO_0000203 NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- befree-2016 importedOn "2016-02-19" NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.