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- source_evidence_literature type ECO_0000212 NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_provenance.
- NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_assertion description "[LOH was observed at 3p21, 17p13(TP53), or in multiple chromosomal arms significantly more often in SCC than in normal epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_provenance.
- NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_assertion evidence source_evidence_literature NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_provenance.
- NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_assertion SIO_000772 11448911 NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_provenance.
- NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_assertion wasDerivedFrom befree-20150227 NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_provenance.
- NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_assertion wasGeneratedBy ECO_0000203 NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP751901.RA_HEULTTFYtyYEETiob5ehCJnifBWXS8CRHwD7OxTIvk130_provenance.