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- source_evidence_literature type ECO_0000212 NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_provenance.
- NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_assertion description "[Today, more than 60 mutations in the factor XIIIA- and B-subunit genes are known leading to congenital factor XIII deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_provenance.
- NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_assertion evidence source_evidence_literature NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_provenance.
- NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_assertion SIO_000772 16543965 NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_provenance.
- NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_assertion wasDerivedFrom befree-20150227 NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_provenance.
- NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_assertion wasGeneratedBy ECO_0000203 NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP392862.RAWplPQZLTrxqUAaN4jLlASDchPOMU8H9wmK2EscWm0Zw130_provenance.