Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance.
- NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_assertion description "[We review the scanty literature data on the association of Cowden syndrome and autism and emphasize that the association of progressive macrocephaly and pervasive developmental disorder seems to be an indication for screening for PTEN mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance.
- NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_assertion evidence source_evidence_literature NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance.
- NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_assertion SIO_000772 11496368 NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance.
- NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_assertion wasDerivedFrom befree-20140225 NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance.
- NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_assertion wasGeneratedBy ECO_0000203 NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP642619.RAA6N2hxqeUTOACqpzlxy7a3FzwP5c3UI7887NNt46Up8130_provenance.