Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance.
- NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_assertion description "[Based on rare human mutations in PTEN and the PI3K pathway, the authors suggest they have produced a potential animal model of autism with macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance.
- NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_assertion evidence source_evidence_literature NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance.
- NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_assertion SIO_000772 16675386 NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance.
- NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_assertion wasDerivedFrom befree-20140225 NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance.
- NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_assertion wasGeneratedBy ECO_0000203 NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP433028.RA5FbepvCwzErzq1-HJI-02WiUTlLrZJtopZ0HtahtvvU130_provenance.