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- source_evidence_literature type ECO_0000212 NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_provenance.
- NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_assertion description "[A genetic mutation within its MSP domain, P56S, was identified in familial forms of motor neuron diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_provenance.
- NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_assertion evidence source_evidence_literature NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_provenance.
- NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_assertion SIO_000772 20207736 NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_provenance.
- NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_assertion wasDerivedFrom befree-20150227 NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_provenance.
- NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_assertion wasGeneratedBy ECO_0000203 NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP570946.RAaQuWWnFE5e_UTGt5ZpnAYHZT6VUAPLbl3vhblD5thOk130_provenance.