Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance.
- NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_assertion description "[They indicate that germline mutations in LZTR1 confer an increased risk of vestibular schwannoma, providing further overlap with NF2, and that further causative genes for schwannomatosis remain to be identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance.
- NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_assertion evidence source_evidence_literature NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance.
- NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_assertion SIO_000772 25480913 NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance.
- NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_assertion wasDerivedFrom befree-2016 NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance.
- NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_assertion wasGeneratedBy ECO_0000203 NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245381.RAyiHwE99dC4DDtcCIblBZbrD79pcFAhmQdpMVnLmEr4w130_provenance.