Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance.
- NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_assertion description "[This is the first report showing loss of heterozygosity at the intron 1 region of p53 gene in human brain tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance.
- NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_assertion evidence source_evidence_literature NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance.
- NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_assertion SIO_000772 17180249 NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance.
- NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_assertion wasDerivedFrom lhgdn-20090331 NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance.
- NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_assertion wasGeneratedBy ECO_0000203 NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP221585.RAkU30LP0V9Vr_2cGiaCVPaSKvL6acpxeWXZ0rYWkRZPI130_provenance.