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- source_evidence_literature type ECO_0000212 NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_provenance.
- NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_assertion description "[Mutations within the RIEG1 homeobox gene on chromosome 4q25 have previously been reported in association with Rieger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_provenance.
- NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_assertion evidence source_evidence_literature NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_provenance.
- NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_assertion SIO_000772 10051017 NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_provenance.
- NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_assertion wasDerivedFrom befree-20140225 NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_provenance.
- NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_assertion wasGeneratedBy ECO_0000203 NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401628.RA81O3o6JUZG7sMILi9W4a_Q71w4RAVndTdN0fudrmrf4130_provenance.