Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance.
- NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_assertion description "[Screening of PTEN mutations is warranted in patients with autism and pronounced macrocephaly, even in the absence of other features of PTEN-related tumor syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance.
- NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_assertion evidence source_evidence_literature NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance.
- NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_assertion SIO_000772 17427195 NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance.
- NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_assertion wasDerivedFrom gad-20150221 NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance.
- NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_assertion wasGeneratedBy ECO_0000203 NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP65727.RA1sfWRYBZf9dnxtFZwQxCV7o3wCBVrdS5xCCT9L0pGQI130_provenance.