Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance.
- NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_assertion description "[In addition, a germline PTEN mutation was identified in a male with hemimegalencephaly but no peripheral manifestations of the PTEN hamartoma tumour syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance.
- NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_assertion evidence source_evidence_literature NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance.
- NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_assertion SIO_000772 25722288 NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance.
- NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_assertion wasDerivedFrom befree-2016 NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance.
- NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_assertion wasGeneratedBy ECO_0000203 NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266695.RAfxVXcPyt5h8dg_IifapufVR9vzYKF-xE5KVhV6soKF8130_provenance.