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- source_evidence_literature type ECO_0000212 NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_provenance.
- NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_assertion wasGeneratedBy ECO_0000203 NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_provenance.
- NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_assertion wasDerivedFrom befree-20150227 NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_provenance.
- NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_assertion SIO_000772 22152678 NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_provenance.
- NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_assertion evidence source_evidence_literature NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_provenance.
- NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_assertion description "[We used whole-exome sequencing of five unrelated individuals with lepto-SEMDJL to identify mutations in KIF22 as the cause of this skeletal condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526826.RAqNrERBrPhSdPS2Jzm1Ea3TRWuRuGracrn5fPcaN5DYc130_provenance.