Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance.
- NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_assertion description "[Similarly, human HS showed genetic or epigenetic inactivation of PTEN, p16(INK4A), and p14(ARF), supporting the relevance of this genetically engineered mouse model of HS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance.
- NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_assertion evidence source_evidence_literature NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance.
- NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_assertion SIO_000772 16697958 NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance.
- NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_assertion wasDerivedFrom befree-20140225 NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance.
- NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_assertion wasGeneratedBy ECO_0000203 NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance.
- befree-20140225 importedOn "2014-02-25" NP250155.RAEn_jp5OhcPBB4ulqeKSf0glN1gUSLmeQD1svCtl66ls130_provenance.