Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.
- NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_assertion description "[16 patients from 11 unrelated families were studied with a phenotype of infantile ascending hereditary spastic paralysis (IAHSP); Alsin mutations were found in 4 of the 10 families, whereas haplotype analysis excluded the ALS2 locus in one family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.
- NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_assertion evidence source_evidence_literature NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.
- NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_assertion SIO_000772 12601111 NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.
- NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_assertion wasDerivedFrom lhgdn-20090331 NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.
- NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_assertion wasGeneratedBy ECO_0000203 NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198337.RAUsxADcbWizL9EnFd41Mc_7QLpfMcd5YzYK7-NdlSYHE130_provenance.